Showing 831 items.
- Bipolar disorder (transclusion) (links | )
- Charcot–Marie–Tooth disease (transclusion) (links | )
- Essential tremor (transclusion) (links | )
- Haemophilia (transclusion) (links | )
- Muscular dystrophy (transclusion) (links | )
- Autosomal dominant polycystic kidney disease (transclusion) (links | )
- Superoxide dismutase (transclusion) (links | )
- Stuttering (transclusion) (links | )
- Von Hippel–Lindau disease (transclusion) (links | )
- Brown (transclusion) (links | )
- Anthrax (transclusion) (links | )
- Leprosy (transclusion) (links | )
- Epigenetics (transclusion) (links | )
- Cystic fibrosis (transclusion) (links | )
- Cerebral palsy (transclusion) (links | )
- Sodium cyanide (transclusion) (links | )
- Androgen insensitivity syndrome (transclusion) (links | )
- Adrenoleukodystrophy (transclusion) (links | )
- Prader–Willi syndrome (transclusion) (links | )
- Blood type (transclusion) (links | )
- Gout (transclusion) (links | )
- Canavan disease (transclusion) (links | )
- Joubert syndrome (transclusion) (links | )
- Neurofibromatosis (transclusion) (links | )
- Tay–Sachs disease (transclusion) (links | )
- Achondroplasia (transclusion) (links | )
- Dominance (genetics) (transclusion) (links | )
- Glaucoma (transclusion) (links | )
- Brachydactyly (transclusion) (links | )
- Myoglobin (transclusion) (links | )
- Cenani–Lenz syndactylism (transclusion) (links | )
- Xanthine oxidase (transclusion) (links | )
- Febrile seizure (transclusion) (links | )
- Brugada syndrome (transclusion) (links | )
- Ehlers–Danlos syndrome (transclusion) (links | )
- Congenital disorder of glycosylation (transclusion) (links | )
- Polydactyly (transclusion) (links | )
- Bladder cancer (transclusion) (links | )
- Langer–Giedion syndrome (transclusion) (links | )
- Hair loss (transclusion) (links | )
- Mydriasis (transclusion) (links | )
- Toe (transclusion) (links | )
- Lissencephaly (transclusion) (links | )
- Hereditary spastic paraplegia (transclusion) (links | )
- Cleft lip and cleft palate (transclusion) (links | )
- Restless legs syndrome (transclusion) (links | )
- Otosclerosis (transclusion) (links | )
- Multiple endocrine neoplasia (transclusion) (links | )
- Thalassemia (transclusion) (links | )
- Hirschsprung's disease (transclusion) (links | )
- Tietz syndrome (transclusion) (links | )
- Follicle-stimulating hormone (transclusion) (links | )
- Congenital hypothyroidism (transclusion) (links | )
- Retinitis pigmentosa (transclusion) (links | )
- Long QT syndrome (transclusion) (links | )
- Limb–girdle muscular dystrophy (transclusion) (links | )
- Weissenbacher–Zweymüller syndrome (transclusion) (links | )
- Renal cell carcinoma (transclusion) (links | )
- Spinal muscular atrophies (transclusion) (links | )
- Actin (transclusion) (links | )
- Occipital horn syndrome (transclusion) (links | )
- Cytochrome C1 (transclusion) (links | )
- Familial Mediterranean fever (transclusion) (links | )
- Hereditary spherocytosis (transclusion) (links | )
- Congenital adrenal hyperplasia (transclusion) (links | )
- Hypercalcaemia (transclusion) (links | )
- Galactosemia (transclusion) (links | )
- Porphyria cutanea tarda (transclusion) (links | )
- Thrombopoietin (transclusion) (links | )
- Osteopetrosis (transclusion) (links | )
- HLA-B27 (transclusion) (links | )
- Mucopolysaccharidosis (transclusion) (links | )
- Iron overload (transclusion) (links | )
- Methylmalonic acidemias (transclusion) (links | )
- Propionic acidemia (transclusion) (links | )
- Hyperammonemia (transclusion) (links | )
- Wilms' tumor (transclusion) (links | )
- XY gonadal dysgenesis (transclusion) (links | )
- Gaucher's disease (transclusion) (links | )
- Dichromacy (transclusion) (links | )
- Tuberous sclerosis (transclusion) (links | )
- Arrhythmogenic cardiomyopathy (transclusion) (links | )
- Hypertrophic cardiomyopathy (transclusion) (links | )
- Dilated cardiomyopathy (transclusion) (links | )
- Ichthyosis (transclusion) (links | )
- Congenital insensitivity to pain (transclusion) (links | )
- Waardenburg syndrome (transclusion) (links | )
- Lamellar ichthyosis (transclusion) (links | )
- Phenylthiocarbamide (transclusion) (links | )
- Potassium cyanide (transclusion) (links | )
- Short QT syndrome (transclusion) (links | )
- Wiskott–Aldrich syndrome protein (transclusion) (links | )
- Chronic granulomatous disease (transclusion) (links | )
- Primary ciliary dyskinesia (transclusion) (links | )
- Paget's disease of bone (transclusion) (links | )
- Dystonia (transclusion) (links | )
- Autoimmune polyendocrine syndrome (transclusion) (links | )
- Homocystinuria (transclusion) (links | )
- Epidermolysis bullosa (transclusion) (links | )
- Frontotemporal dementia (transclusion) (links | )
- Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency (transclusion) (links | )
- IgA nephropathy (transclusion) (links | )
- Hereditary hemorrhagic telangiectasia (transclusion) (links | )
- Alport syndrome (transclusion) (links | )
- Hereditary fructose intolerance (transclusion) (links | )
- Hypopituitarism (transclusion) (links | )
- Eye color (transclusion) (links | )
- Beckwith–Wiedemann syndrome (transclusion) (links | )
- Niemann–Pick disease (transclusion) (links | )
- Sanfilippo syndrome (transclusion) (links | )
- Glanzmann's thrombasthenia (transclusion) (links | )
- Aniridia (transclusion) (links | )
- Hyperhidrosis (transclusion) (links | )
- Renal agenesis (transclusion) (links | )
- Osteogenesis imperfecta (transclusion) (links | )
- Maturity-onset diabetes of the young (transclusion) (links | )
- Alexander disease (transclusion) (links | )
- Plasmin (transclusion) (links | )
- Usher syndrome (transclusion) (links | )
- Angioedema (transclusion) (links | )
- Hyperinsulinemic hypoglycemia (transclusion) (links | )
- Asplenia (transclusion) (links | )
- Arthrogryposis (transclusion) (links | )
- Duchenne muscular dystrophy (transclusion) (links | )
- Familial thoracic aortic aneurysm (transclusion) (links | )
- Noonan syndrome (transclusion) (links | )
- Gardner's syndrome (transclusion) (links | )
- Transglutaminase (transclusion) (links | )
- Hereditary multiple exostoses (transclusion) (links | )
- Cystinuria (transclusion) (links | )
- Hyperkalemic periodic paralysis (transclusion) (links | )
- Pyruvate kinase deficiency (transclusion) (links | )
- Situs ambiguus (transclusion) (links | )
- Thyroid hormone resistance (transclusion) (links | )
- Wolf–Hirschhorn syndrome (transclusion) (links | )
- Kallmann syndrome (transclusion) (links | )
- Lesch–Nyhan syndrome (transclusion) (links | )
- Gunther disease (transclusion) (links | )
- Menkes disease (transclusion) (links | )
- Immunodeficiency–centromeric instability–facial anomalies syndrome (transclusion) (links | )
- Chorea-acanthocytosis (transclusion) (links | )
- Berdon syndrome (transclusion) (links | )
- Alopecia universalis (transclusion) (links | )
- Zellweger syndrome (transclusion) (links | )
- Potter sequence (transclusion) (links | )
- Xeroderma pigmentosum (transclusion) (links | )
- Pemphigus (transclusion) (links | )
- Bloom syndrome (transclusion) (links | )
- Hereditary nonpolyposis colorectal cancer (transclusion) (links | )
- Cream gene (transclusion) (links | )
- Olivopontocerebellar atrophy (transclusion) (links | )
- Equine coat color genetics (transclusion) (links | )
- Glial fibrillary acidic protein (transclusion) (links | )
- Chromosome 5q deletion syndrome (transclusion) (links | )
- Palmoplantar keratoderma (transclusion) (links | )
- Nesidioblastosis (transclusion) (links | )
- Arachnoiditis (transclusion) (links | )
- Müllerian agenesis (transclusion) (links | )
- Supertaster (transclusion) (links | )
- Microcephalin (transclusion) (links | )
- Progressive supranuclear palsy (transclusion) (links | )
- Hypodontia (transclusion) (links | )
- Mismatch repair cancer syndrome (transclusion) (links | )
- Fukuyama congenital muscular dystrophy (transclusion) (links | )
- Cockayne syndrome (transclusion) (links | )
- Rubinstein–Taybi syndrome (transclusion) (links | )
- Jervell and Lange-Nielsen syndrome (transclusion) (links | )
- Langerhans cell (transclusion) (links | )
- Romano–Ward syndrome (transclusion) (links | )
- Andersen–Tawil syndrome (transclusion) (links | )
- Craniosynostosis (transclusion) (links | )
- Hyperlipidemia (transclusion) (links | )
- Beta-secretase 2 (transclusion) (links | )
- Mulibrey nanism (transclusion) (links | )
- Stickler syndrome (transclusion) (links | )
- Titin (transclusion) (links | )
- Fuchs' dystrophy (transclusion) (links | )
- Neurofibromatosis type I (transclusion) (links | )
- Glycogen storage disease type I (transclusion) (links | )
- Duane syndrome (transclusion) (links | )
- Glycine receptor (transclusion) (links | )
- Isovaleric acidemia (transclusion) (links | )
- Maple syrup urine disease (transclusion) (links | )
- Nude mouse (transclusion) (links | )
- X-linked ichthyosis (transclusion) (links | )
- Achondrogenesis (transclusion) (links | )
- Leber's hereditary optic neuropathy (transclusion) (links | )
- Cystinosis (transclusion) (links | )
- Nemaline myopathy (transclusion) (links | )
- Citrullinemia (transclusion) (links | )
- Amyloid beta (transclusion) (links | )
- Congenital diaphragmatic hernia (transclusion) (links | )
- Klippel–Feil syndrome (transclusion) (links | )
- Syndactyly (transclusion) (links | )
- Prognathism (transclusion) (links | )
- Fas ligand (transclusion) (links | )
- Xanthinuria (transclusion) (links | )
- Tyrosinemia (transclusion) (links | )
- Systemic primary carnitine deficiency (transclusion) (links | )
- Meleda disease (transclusion) (links | )
- Atresia (transclusion) (links | )
- Netrin (transclusion) (links | )
- Neuronal ceroid lipofuscinosis (transclusion) (links | )
- Imperforate anus (transclusion) (links | )
- Van der Woude syndrome (transclusion) (links | )
- Focal segmental glomerulosclerosis (transclusion) (links | )
- Spinocerebellar ataxia (transclusion) (links | )
- Microtia (transclusion) (links | )
- ADAMTS13 (transclusion) (links | )
- Primary hyperparathyroidism (transclusion) (links | )
- ABL (gene) (transclusion) (links | )
- Calcium pyrophosphate dihydrate crystal deposition disease (transclusion) (links | )
- Hartnup disease (transclusion) (links | )
- DNA mismatch repair (transclusion) (links | )
- Intestinal neuronal dysplasia (transclusion) (links | )
- Sandhoff disease (transclusion) (links | )
- Carnitine palmitoyltransferase II deficiency (transclusion) (links | )
- Morquio syndrome (transclusion) (links | )
- Severe congenital neutropenia (transclusion) (links | )
- Saccharopinuria (transclusion) (links | )
- Salla disease (transclusion) (links | )
- Facioscapulohumeral muscular dystrophy (transclusion) (links | )
- Spondyloperipheral dysplasia (transclusion) (links | )
- Multiple endocrine neoplasia type 2 (transclusion) (links | )
- Hypophosphatasia (transclusion) (links | )
- Cowden syndrome (transclusion) (links | )
- Lysinuric protein intolerance (transclusion) (links | )
- Sideroblastic anemia (transclusion) (links | )
- Bullous pemphigoid (transclusion) (links | )
- Leukocyte adhesion deficiency (transclusion) (links | )
- Hypogammaglobulinemia (transclusion) (links | )
- Carpenter syndrome (transclusion) (links | )
- Myelin oligodendrocyte glycoprotein (transclusion) (links | )
- Hemopexin (transclusion) (links | )
- Transforming growth factor beta (transclusion) (links | )
- Periodic paralysis (transclusion) (links | )
- Tissue factor (transclusion) (links | )
- Glycogen storage disease type IV (transclusion) (links | )
- Glycogen storage disease type III (transclusion) (links | )
- Glycogen storage disease type 0 (transclusion) (links | )
- Hereditary elliptocytosis (transclusion) (links | )
- Common variable immunodeficiency (transclusion) (links | )
- Diamond–Blackfan anemia (transclusion) (links | )
- Dyskeratosis congenita (transclusion) (links | )
- Tissue factor pathway inhibitor (transclusion) (links | )
- Hyperaldosteronism (transclusion) (links | )
- Pure red cell aplasia (transclusion) (links | )
- Crigler–Najjar syndrome (transclusion) (links | )
- WAGR syndrome (transclusion) (links | )
- Neural tube defect (transclusion) (links | )
- Tachykinin peptides (transclusion) (links | )
- Hypergammaglobulinemia (transclusion) (links | )
- Heritability of autism (transclusion) (links | )
- Pachygyria (transclusion) (links | )
- Pachydermoperiostosis (transclusion) (links | )
- Walker–Warburg syndrome (transclusion) (links | )
- Hypokalemic periodic paralysis (transclusion) (links | )
- Chromosome 11 (transclusion) (links | )
- Nonsyndromic deafness (transclusion) (links | )
- Chromosome 19 (transclusion) (links | )
- Crouzonodermoskeletal syndrome (transclusion) (links | )
- Hermansky–Pudlak syndrome (transclusion) (links | )
- Nephrogenic diabetes insipidus (transclusion) (links | )
- Hereditary stomatocytosis (transclusion) (links | )
- Collagen, type I, alpha 1 (transclusion) (links | )
- Pseudohypoparathyroidism (transclusion) (links | )
- Huntingtin (transclusion) (links | )
- MUTYH (transclusion) (links | )
- Oculocutaneous albinism (transclusion) (links | )
- Collagen, type XI, alpha 2 (transclusion) (links | )
- TBX1 (transclusion) (links | )
- HLA-B (transclusion) (links | )
- IKBKAP (transclusion) (links | )
- Bernard–Soulier syndrome (transclusion) (links | )
- Nijmegen breakage syndrome (transclusion) (links | )
- Asymmetric crying facies (transclusion) (links | )
- Familial male-limited precocious puberty (transclusion) (links | )
- Fountain syndrome (transclusion) (links | )
- ZAP70 deficiency (transclusion) (links | )
- Chestnut (horse color) (transclusion) (links | )
- Pacman dysplasia (transclusion) (links | )
- Phosphoinositide 3-kinase (transclusion) (links | )
- Ayazi syndrome (transclusion) (links | )
- Glucocorticoid deficiency 1 (transclusion) (links | )
- 2-Hydroxyglutaric aciduria (transclusion) (links | )
- Malonic aciduria (transclusion) (links | )
- 3-Methylglutaconic aciduria (transclusion) (links | )
- Short-chain acyl-coenzyme A dehydrogenase deficiency (transclusion) (links | )
- 3-Methylcrotonyl-CoA carboxylase deficiency (transclusion) (links | )
- Methylmalonyl-CoA mutase deficiency (transclusion) (links | )
- Carney complex (transclusion) (links | )
- Zaspopathy (transclusion) (links | )
- Bartter syndrome (transclusion) (links | )
- Pax genes (transclusion) (links | )
- Adenylosuccinate lyase deficiency (transclusion) (links | )
- Simpson–Golabi–Behmel syndrome (transclusion) (links | )
- Autosomal recessive multiple epiphyseal dysplasia (transclusion) (links | )
- Progressive familial intrahepatic cholestasis (transclusion) (links | )
- Familial hemiplegic migraine (transclusion) (links | )
- Alpha-thalassemia (transclusion) (links | )
- Arakawa's syndrome II (transclusion) (links | )
- Factor XIII deficiency (transclusion) (links | )
- Cytochrome b5 (transclusion) (links | )
- Apolipoprotein E (transclusion) (links | )
- Triple-A syndrome (transclusion) (links | )
- Drusen (transclusion) (links | )
- Hyperimmunoglobulin E syndrome (transclusion) (links | )
- Hyperekplexia (transclusion) (links | )
- Hajdu–Cheney syndrome (transclusion) (links | )
- Griscelli syndrome (transclusion) (links | )
- X-linked severe combined immunodeficiency (transclusion) (links | )
- Fumarase deficiency (transclusion) (links | )
- Seckel syndrome (transclusion) (links | )
- Selective immunoglobulin A deficiency (transclusion) (links | )
- Refsum disease (transclusion) (links | )
- Primary ovarian insufficiency (transclusion) (links | )
- Balkan endemic nephropathy (transclusion) (links | )
- Felty's syndrome (transclusion) (links | )
- Vitelliform macular dystrophy (transclusion) (links | )
- Spermatogenesis arrest (transclusion) (links | )
- Centronuclear myopathy (transclusion) (links | )
- Cutis laxa (transclusion) (links | )
- Freeman–Sheldon syndrome (transclusion) (links | )
- Rotor syndrome (transclusion) (links | )
- Congenital absence of the vas deferens (transclusion) (links | )
- DAB1 (transclusion) (links | )
- Hedgehog signaling pathway (transclusion) (links | )
- Da Costa's syndrome (transclusion) (links | )
- Laurence–Moon syndrome (transclusion) (links | )
- Lucey–Driscoll syndrome (transclusion) (links | )
- Larsen syndrome (transclusion) (links | )
- 2-Methylbutyryl-CoA dehydrogenase deficiency (transclusion) (links | )
- Epidermolysis bullosa simplex (transclusion) (links | )
- HEC syndrome (transclusion) (links | )
- Endocardial fibroelastosis (transclusion) (links | )
- Primordial dwarfism (transclusion) (links | )
- VLDL receptor (transclusion) (links | )
- ATR-X syndrome (transclusion) (links | )
- Alström syndrome (transclusion) (links | )
- Autosomal dominant hypophosphatemic rickets (transclusion) (links | )
- UDP glucuronosyltransferase 1 family, polypeptide A1 (transclusion) (links | )
- Agouti-signaling protein (transclusion) (links | )
- Acromicric dysplasia (transclusion) (links | )
- Kell antigen system (transclusion) (links | )
- Kidd antigen system (transclusion) (links | )
- Colton antigen system (transclusion) (links | )
- Nezelof syndrome (transclusion) (links | )
- Yt antigen system (transclusion) (links | )
- Pseudohypoaldosteronism (transclusion) (links | )
- G protein-coupled receptor kinase (transclusion) (links | )
- Emery–Dreifuss muscular dystrophy (transclusion) (links | )
- XX gonadal dysgenesis (transclusion) (links | )
- Spinal muscular atrophy (transclusion) (links | )
- TGF beta signaling pathway (transclusion) (links | )
- Peroxisomal disorder (transclusion) (links | )
- Thiamine deficiency (transclusion) (links | )
- Prekallikrein (transclusion) (links | )
- GM2 gangliosidoses (transclusion) (links | )
- GM1 gangliosidoses (transclusion) (links | )
- MERRF syndrome (transclusion) (links | )
- Autoimmune lymphoproliferative syndrome (transclusion) (links | )
- Fazio–Londe disease (transclusion) (links | )
- Chin (transclusion) (links | )
- Vesicular transport adaptor protein (transclusion) (links | )
- Short rib–polydactyly syndrome (transclusion) (links | )
- Partial androgen insensitivity syndrome (transclusion) (links | )
- Catel–Manzke syndrome (transclusion) (links | )
- Distal myopathy (transclusion) (links | )
- Acatalasia (transclusion) (links | )
- Lipoatrophic diabetes (transclusion) (links | )
- Papillon–Lefèvre syndrome (transclusion) (links | )
- Noonan syndrome with multiple lentigines (transclusion) (links | )
- Bare lymphocyte syndrome (transclusion) (links | )
- Intestinal atresia (transclusion) (links | )
- Ataxin 7 (transclusion) (links | )
- Chronic intestinal pseudo-obstruction (transclusion) (links | )
- Familial amyloid polyneuropathy (transclusion) (links | )
- Down syndrome research (transclusion) (links | )
- Periodic fever syndrome (transclusion) (links | )
- Loeys–Dietz syndrome (transclusion) (links | )
- Neonatal-onset multisystem inflammatory disease (transclusion) (links | )
- 1p36 deletion syndrome (transclusion) (links | )
- X-linked hypophosphatemia (transclusion) (links | )
- Medullary cystic kidney disease (transclusion) (links | )
- Carbamoyl phosphate synthetase I deficiency (transclusion) (links | )
- Cerebrotendineous xanthomatosis (transclusion) (links | )
- Erythropoietic porphyria (transclusion) (links | )
- Hypohidrotic ectodermal dysplasia (transclusion) (links | )
- Rhizomelic chondrodysplasia punctata (transclusion) (links | )
- Chondrodysplasia punctata (transclusion) (links | )
- Sarcosinemia (transclusion) (links | )
- Axenfeld–Rieger syndrome (transclusion) (links | )
- Fetal hydantoin syndrome (transclusion) (links | )
- Thomas J. Hudson (transclusion) (links | )
- Generalized epilepsy with febrile seizures plus (transclusion) (links | )
- Multiple epiphyseal dysplasia (transclusion) (links | )
- Benign familial neonatal seizures (transclusion) (links | )
- Autosomal dominant nocturnal frontal lobe epilepsy (transclusion) (links | )
- Gray platelet syndrome (transclusion) (links | )
- White sponge nevus (transclusion) (links | )
- Lecithin cholesterol acyltransferase deficiency (transclusion) (links | )
- Hemophagocytic lymphohistiocytosis (transclusion) (links | )
- Specific granule (transclusion) (links | )
- Catecholaminergic polymorphic ventricular tachycardia (transclusion) (links | )
- Mevalonate kinase deficiency (transclusion) (links | )
- Papillorenal syndrome (transclusion) (links | )
- Branchio-oto-renal syndrome (transclusion) (links | )
- Episodic ataxia (transclusion) (links | )
- Congenital nephrotic syndrome (transclusion) (links | )
- RAPADILINO syndrome (transclusion) (links | )
- Congenital stationary night blindness (transclusion) (links | )
- Ornithine translocase deficiency (transclusion) (links | )
- Mannan-binding lectin (transclusion) (links | )
- Polycystic liver disease (transclusion) (links | )
- Laron syndrome (transclusion) (links | )
- Naegeli–Franceschetti–Jadassohn syndrome (transclusion) (links | )
- Timeline of tuberous sclerosis (transclusion) (links | )
- Optic disc drusen (transclusion) (links | )
- Familial atrial fibrillation (transclusion) (links | )
- Hay–Wells syndrome (transclusion) (links | )
- Antithrombin III deficiency (transclusion) (links | )
- Laminopathy (transclusion) (links | )
- Pachyonychia congenita (transclusion) (links | )
- Dent's disease (transclusion) (links | )
- Meckel–Gruber syndrome (transclusion) (links | )
- Thyroid dyshormonogenesis (transclusion) (links | )
- Pyruvate dehydrogenase kinase (transclusion) (links | )
- Troponin C (transclusion) (links | )
- Troponin T (transclusion) (links | )
- Troponin I (transclusion) (links | )
- Membranoproliferative glomerulonephritis (transclusion) (links | )
- 3-Hydroxy-3-methylglutaryl-CoA lyase (transclusion) (links | )
- Oguchi disease (transclusion) (links | )
- Wallis–Zieff–Goldblatt syndrome (transclusion) (links | )
- OCRL (transclusion) (links | )
- Prelamin-A/C (transclusion) (links | )
- Lamin B receptor (transclusion) (links | )
- May–Hegglin anomaly (transclusion) (links | )
- Samuel Gee (transclusion) (links | )
- Ribosomal s6 kinase (transclusion) (links | )
- Epidermodysplasia verruciformis (transclusion) (links | )
- Pipecolic acidemia (transclusion) (links | )
- Galactokinase deficiency (transclusion) (links | )
- Aldolase A deficiency (transclusion) (links | )
- Lipoprotein lipase deficiency (transclusion) (links | )
- Paroxysmal nonkinesigenic dyskinesia (transclusion) (links | )
- 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (transclusion) (links | )
- RET proto-oncogene (transclusion) (links | )
- Zonular cataract and nystagmus (transclusion) (links | )
- Zori–Stalker–Williams syndrome (transclusion) (links | )
- Yunis–Varon syndrome (transclusion) (links | )
- Purine nucleoside phosphorylase deficiency (transclusion) (links | )
- Doublecortin (transclusion) (links | )
- Mevalonate kinase (transclusion) (links | )
- 3C syndrome (transclusion) (links | )
- Pyridoxine 5′-phosphate oxidase (transclusion) (links | )
- Dubowitz syndrome (transclusion) (links | )
- Acetylserotonin O-methyltransferase (transclusion) (links | )
- Galactose epimerase deficiency (transclusion) (links | )
- Essential fructosuria (transclusion) (links | )
- Uncombable hair syndrome (transclusion) (links | )
- Upington disease (transclusion) (links | )
- Urban–Rogers–Meyer syndrome (transclusion) (links | )
- Galactose-1-phosphate uridylyltransferase deficiency (transclusion) (links | )
- TCF7L2 (transclusion) (links | )
- Complement deficiency (transclusion) (links | )
- Snatiation (transclusion) (links | )
- Orotic aciduria (transclusion) (links | )
- Fumarylacetoacetate hydrolase (transclusion) (links | )
- Cystathioninuria (transclusion) (links | )
- N-acetylglucosamine-1-phosphate transferase (transclusion) (links | )
- Cornelia de Lange syndrome (transclusion) (links | )
- ETV6 (transclusion) (links | )
- Leukoencephalopathy with vanishing white matter (transclusion) (links | )
- Young's syndrome (transclusion) (links | )
- Sulfate transporter (transclusion) (links | )
- Vici syndrome (transclusion) (links | )
- Epidermolysis bullosa dystrophica (transclusion) (links | )
- Infantile Refsum disease (transclusion) (links | )
- Neonatal adrenoleukodystrophy (transclusion) (links | )
- Bietti's crystalline dystrophy (transclusion) (links | )
- KLF1 (transclusion) (links | )
- Spastic quadriplegia (transclusion) (links | )
- Electron-transferring-flavoprotein dehydrogenase (transclusion) (links | )
- Rothmund–Thomson syndrome (transclusion) (links | )
- Buschke–Ollendorff syndrome (transclusion) (links | )
- Fukutin (transclusion) (links | )
- VPS13B (transclusion) (links | )
- Senior–Løken syndrome (transclusion) (links | )
- CAMFAK syndrome (transclusion) (links | )
- Brunner syndrome (transclusion) (links | )
- TRPV4 (transclusion) (links | )
- Hereditary neuralgic amyotrophy (transclusion) (links | )
- Spondylocostal dysostosis (transclusion) (links | )
- GJB1 (transclusion) (links | )
- Fibrillin-1 (transclusion) (links | )
- MEF2C (transclusion) (links | )
- LAMP2 (transclusion) (links | )
- HK1 (transclusion) (links | )
- Marshall–Smith syndrome (transclusion) (links | )
- Hypervalinemia (transclusion) (links | )
- Sequestosome 1 (transclusion) (links | )
- Collagen, type VII, alpha 1 (transclusion) (links | )
- Ohtahara syndrome (transclusion) (links | )
- Cutis verticis gyrata (transclusion) (links | )
- Lactate dehydrogenase (transclusion) (links | )
- Cytochrome c oxidase subunit I (transclusion) (links | )
- GJB6 (transclusion) (links | )
- RIPK1 (transclusion) (links | )
- Interferon gamma receptor 1 (transclusion) (links | )
- NT5E (transclusion) (links | )
- SAT1 (gene) (transclusion) (links | )
- Enolase 2 (transclusion) (links | )
- H19 (gene) (transclusion) (links | )
- KCNJ5 (transclusion) (links | )
- CLCN2 (transclusion) (links | )
- Tubulin beta-4A chain (transclusion) (links | )
- Twinkle (protein) (transclusion) (links | )
- PACS1 (transclusion) (links | )
- Ectodysplasin A receptor (transclusion) (links | )
- ATP13A2 (transclusion) (links | )
- CYP4F2 (transclusion) (links | )
- POMT1 (transclusion) (links | )
- Phosphate carrier protein, mitochondrial (transclusion) (links | )
- TFAP2A (transclusion) (links | )
- COX10 (transclusion) (links | )
- CA8 (transclusion) (links | )
- Mitochondrial dicarboxylate carrier (transclusion) (links | )
- PHF8 (transclusion) (links | )
- UQCRC2 (transclusion) (links | )
- ATG7 (transclusion) (links | )
- TBX22 (transclusion) (links | )
- GON4L (transclusion) (links | )
- CD79A (transclusion) (links | )
- Revesz syndrome (transclusion) (links | )
- Camurati–Engelmann disease (transclusion) (links | )
- X-linked lymphoproliferative disease (transclusion) (links | )
- Primary hyperoxaluria (transclusion) (links | )
- Weill–Marchesani syndrome (transclusion) (links | )
- Woodhouse–Sakati syndrome (transclusion) (links | )
- Antley–Bixler syndrome (transclusion) (links | )
- Beta-mannosidosis (transclusion) (links | )
- ETFDH (transclusion) (links | )
- TMEM8B (transclusion) (links | )
- SCN7A (transclusion) (links | )
- Galactosemic cataract (transclusion) (links | )
- Carnosinemia (transclusion) (links | )
- Acrocallosal syndrome (transclusion) (links | )
- Hypoalphalipoproteinemia (transclusion) (links | )
- Epiblepharon (transclusion) (links | )
- Diffuse panbronchiolitis (transclusion) (links | )
- 2p15-16.1 microdeletion syndrome (transclusion) (links | )
- 3-M syndrome (transclusion) (links | )
- Hereditary motor and sensory neuropathy (transclusion) (links | )
- Hereditary sensory and autonomic neuropathy (transclusion) (links | )
- Chronic mucocutaneous candidiasis (transclusion) (links | )
- Juvenile hemochromatosis (transclusion) (links | )
- Ocular albinism (transclusion) (links | )
- Ciliopathy (transclusion) (links | )
- Marden–Walker syndrome (transclusion) (links | )
- Orofaciodigital syndrome 1 (transclusion) (links | )
- Intellectual disability (transclusion) (links | )
- Oculocutaneous albinism type I (transclusion) (links | )
- Brown–Vialetto–Van Laere syndrome (transclusion) (links | )
- Fibrochondrogenesis (transclusion) (links | )
- Gerodermia osteodysplastica (transclusion) (links | )
- Niemann–Pick disease type C (transclusion) (links | )
- SMPD1-associated Niemann–Pick disease (transclusion) (links | )
- Serpentine fibula–polycystic kidney syndrome (transclusion) (links | )
- Schindler disease (transclusion) (links | )
- Ichthyosis bullosa of Siemens (transclusion) (links | )
- Hypertryptophanemia (transclusion) (links | )
- FG syndrome (transclusion) (links | )
- Chilblain lupus erythematosus (transclusion) (links | )
- Ichthyosis hystrix (transclusion) (links | )
- Keratitis–ichthyosis–deafness syndrome (transclusion) (links | )
- Infantile systemic hyalinosis (transclusion) (links | )
- Angioma serpiginosum (transclusion) (links | )
- Iminoglycinuria (transclusion) (links | )
- Aplasia cutis congenita (transclusion) (links | )
- Tetra-amelia syndrome (transclusion) (links | )
- Roundabout family (transclusion) (links | )
- Confluent and reticulated papillomatosis (transclusion) (links | )
- Trichothiodystrophy (transclusion) (links | )
- Peeling skin syndrome (transclusion) (links | )
- Disseminated superficial actinic porokeratosis (transclusion) (links | )
- Junctional epidermolysis bullosa (medicine) (transclusion) (links | )
- Synpolydactyly (transclusion) (links | )
- Mandibuloacral dysplasia (transclusion) (links | )
- Meesmann corneal dystrophy (transclusion) (links | )
- Familial cirrhosis (transclusion) (links | )
- Acropectoral syndrome (transclusion) (links | )
- Congenital generalized lipodystrophy (transclusion) (links | )
- Familial partial lipodystrophy (transclusion) (links | )
- Worth syndrome (transclusion) (links | )
- Familial hypocalciuric hypercalcemia (transclusion) (links | )
- Parkinson's disease (transclusion) (links | )
- Gillespie syndrome (transclusion) (links | )
- Slit (protein) (transclusion) (links | )
- Pashayan syndrome (transclusion) (links | )
- Johanson–Blizzard syndrome (transclusion) (links | )
- Permanent neonatal diabetes (transclusion) (links | )
- Transient neonatal diabetes (transclusion) (links | )
- Keratolytic winter erythema (transclusion) (links | )
- Inherited patterned lentiginosis (transclusion) (links | )
- Sebaceous adenoma (transclusion) (links | )
- Nakajo syndrome (transclusion) (links | )
- Orofaciodigital syndrome (transclusion) (links | )
- Thiel–Behnke dystrophy (transclusion) (links | )
- Gelatinous drop-like corneal dystrophy (transclusion) (links | )
- Epithelial basement membrane dystrophy (transclusion) (links | )
- Sclerocornea (transclusion) (links | )
- Hyperphenylalaninemia (transclusion) (links | )
- Lujan–Fryns syndrome (transclusion) (links | )
- Potocki–Shaffer syndrome (transclusion) (links | )
- Congenital dyserythropoietic anemia (transclusion) (links | )
- Genetics of obesity (transclusion) (links | )
- Complete androgen insensitivity syndrome (transclusion) (links | )
- Smith–Fineman–Myers syndrome (transclusion) (links | )
- Robert M. Blizzard (transclusion) (links | )
- Rudiger syndrome (transclusion) (links | )
- Lethal congenital contracture syndrome (transclusion) (links | )
- Laryngo-onycho-cutaneous syndrome (transclusion) (links | )
- Stiff skin syndrome (transclusion) (links | )
- Parkes Weber syndrome (transclusion) (links | )
- CBS domain (transclusion) (links | )
- Embryonal rhabdomyosarcoma (transclusion) (links | )
- 8p23.1 duplication syndrome (transclusion) (links | )
- Hereditary mucoepithelial dysplasia (transclusion) (links | )
- Mild androgen insensitivity syndrome (transclusion) (links | )
- Thyrotoxic periodic paralysis (transclusion) (links | )
- Athetoid cerebral palsy (transclusion) (links | )
- Terminal complement pathway deficiency (transclusion) (links | )
- Lattice corneal dystrophy (transclusion) (links | )
- Asphyxiating thoracic dysplasia (transclusion) (links | )
- DNAAF2 (transclusion) (links | )
- Surfactant metabolism dysfunction (transclusion) (links | )
- List of OMIM disorder codes (transclusion) (links | )
- Vesicular glutamate transporter 3 (transclusion) (links | )
- TGM5 (transclusion) (links | )
- Sialuria (transclusion) (links | )
- Coenzyme Q10 deficiency (transclusion) (links | )
- COQ9 (transclusion) (links | )
- PDSS2 (transclusion) (links | )
- Malpuech facial clefting syndrome (transclusion) (links | )
- List of hematologic conditions (transclusion) (links | )
- Granular corneal dystrophy (transclusion) (links | )
- Amelogenesis imperfecta (transclusion) (links | )
- Melanocortin 1 receptor (transclusion) (links | )
- Nasodigitoacoustic syndrome (transclusion) (links | )
- Rh deficiency syndrome (transclusion) (links | )
- Argininemia (transclusion) (links | )
- KLF14 (transclusion) (links | )
- Congenital dyserythropoietic anemia type I (transclusion) (links | )
- Congenital dyserythropoietic anemia type II (transclusion) (links | )
- Congenital dyserythropoietic anemia type III (transclusion) (links | )
- Congenital dyserythropoietic anemia type IV (transclusion) (links | )
- Ectrodactyly (transclusion) (links | )
- NUT carcinoma (transclusion) (links | )
- Donohue syndrome (transclusion) (links | )
- Hereditary diffuse leukoencephalopathy with spheroids (transclusion) (links | )
- Distal hereditary motor neuronopathies (transclusion) (links | )
- Congenital mirror movement disorder (transclusion) (links | )
- Kinesin-like protein KIF11 (transclusion) (links | )
- Hereditary leiomyomatosis and renal cell cancer syndrome (transclusion) (links | )
- Congenital hereditary endothelial dystrophy (transclusion) (links | )
- Spinal muscular atrophy with lower extremity predominance 1 (transclusion) (links | )
- Pontocerebellar hypoplasia (transclusion) (links | )
- Qazi–Markouizos syndrome (transclusion) (links | )
- Parastremmatic dwarfism (transclusion) (links | )
- Focal facial dermal dysplasia (transclusion) (links | )
- Melnick–Needles syndrome (transclusion) (links | )
- Aicardi–Goutières syndrome (transclusion) (links | )
- Tsix (transclusion) (links | )
- Mental retardation and microcephaly with pontine and cerebellar hypoplasia (transclusion) (links | )
- Hereditary sensory and autonomic neuropathy type I (transclusion) (links | )
- Multisystem proteinopathy (transclusion) (links | )
- Young–Madders syndrome (transclusion) (links | )
- Mitochondrial DNA depletion syndrome (transclusion) (links | )
- Kufs disease (transclusion) (links | )
- Primary juvenile glaucoma (transclusion) (links | )
- Cataract-microcornea syndrome (transclusion) (links | )
- Neu–Laxova syndrome (transclusion) (links | )
- Ribosomopathy (transclusion) (links | )
- North American Indian childhood cirrhosis (transclusion) (links | )
- Bowen–Conradi syndrome (transclusion) (links | )
- Epigenetics of neurodegenerative diseases (transclusion) (links | )
- Charcot–Marie–Tooth disease classifications (transclusion) (links | )
- Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A (transclusion) (links | )
- Blue-cone monochromacy (transclusion) (links | )
- Hypotrichosis with juvenile macular dystrophy (transclusion) (links | )
- SLC25A22 (transclusion) (links | )
- MEDNIK syndrome (transclusion) (links | )
- Glucocorticoid deficiency (transclusion) (links | )
- Microlissencephaly (transclusion) (links | )
- Genetics of amyotrophic lateral sclerosis (transclusion) (links | )
- NGLY1 deficiency (transclusion) (links | )
- Vaginal anomalies (transclusion) (links | )
- Genetics of GnRH deficiency conditions (transclusion) (links | )
- Xp11.2 duplication (transclusion) (links | )
- KBG syndrome (transclusion) (links | )
- ANO5 (transclusion) (links | )
- COA6 (transclusion) (links | )
- PET100 (transclusion) (links | )
- PET117 (transclusion) (links | )
- TMEM70 (transclusion) (links | )
- SLC25A46 (transclusion) (links | )
- Cytochrome b5 deficiency (transclusion) (links | )
- Barber–Say syndrome (transclusion) (links | )
- Caudal duplication (transclusion) (links | )
- CARD-CC family (transclusion) (links | )
- Okamoto syndrome (transclusion) (links | )
- Agouti coloration genetics (transclusion) (links | )
- VEXAS syndrome (transclusion) (links | )
- Spinal muscular atrophy with lower extremity predominance 2A (transclusion) (links | )
- Spinal muscular atrophy with lower extremity predominance 2B (transclusion) (links | )
- Isolated growth hormone deficiency (transclusion) (links | )
- Progressive cardiac conduction defect (transclusion) (links | )
- Mitochondrial membrane protein-associated neurodegeneration (transclusion) (links | )
- Congenital red–green color blindness (transclusion) (links | )
- DiGeorge syndrome (transclusion) (links | )
- Methylmalonic acidemia with homocystinuria (transclusion) (links | )
- Talk:Progeria (transclusion) (links | )
- Talk:Adrenoleukodystrophy (transclusion) (links | )
- Talk:Vascular endothelial growth factor (transclusion) (links | )
- Talk:Reye syndrome (transclusion) (links | )
- Talk:Myopathy (transclusion) (links | )
- Talk:Laurence–Moon syndrome (transclusion) (links | )
- Talk:Inhibin (transclusion) (links | )
- Talk:Alcoholism/Archive 1 (transclusion) (links | )
- Talk:Kallmann syndrome (transclusion) (links | )
- Talk:Myopathy/to do (transclusion) (links | )
- Talk:Down syndrome/Archive 4 (transclusion) (links | )
- Talk:Albinism in humans/Humans draft (transclusion) (links | )
- Talk:Hereditary inclusion body myopathy (transclusion) (links | )
- Talk:Fitzsimmons–Guilbert syndrome (transclusion) (links | )
- Talk:Myalgic encephalomyelitis/chronic fatigue syndrome/Archive 4 (transclusion) (links | )
- Talk:Huntington's disease/Archive 2 (transclusion) (links | )
- Talk:Thyrotoxic periodic paralysis (transclusion) (links | )
- Talk:Intellectual disability/Archive 2 (transclusion) (links | )
- Talk:Colorectal cancer/Archive 1 (transclusion) (links | )
- Talk:Wiedemann–Rautenstrauch syndrome (transclusion) (links | )
- Talk:Wilson's disease/Archive 1 (transclusion) (links | )
- Talk:Kallmann syndrome/Archive 1 (transclusion) (links | )
- Talk:Moeschler–Clarren syndrome (transclusion) (links | )
- Talk:Multiple myeloma/Archive 1 (transclusion) (links | )
- Talk:Pena-Shokeir syndrome, type 1 (transclusion) (links | )
- User:Alteripse/workshop2 (transclusion) (links | )
- User:JCraw/Medinfobox (transclusion) (links | )
- User:JCraw/Medinfobox/doc (transclusion) (links | )
- User:Andrew Su/ITK (transclusion) (links | )
- User:Andrew Su/ITK (gene) (transclusion) (links | )
- User:Andrew Su/Template:PBB/3702 (transclusion) (links | )
- User:Frog21/Ltf Version 1 (transclusion) (links | )
- User:Ppgardne/RNA families template (transclusion) (links | )
- User:Frog21/Ltf using MGI Gene box (transclusion) (links | )
- User:Emw/PDBImageTestcases (transclusion) (links | )
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- User:Emw/PDB Sandbox/Animation (transclusion) (links | )
- User:Doctorwolfie/sandbox (transclusion) (links | )
- User:Lindseyboucher/sandbox (transclusion) (links | )
- User:NussPoyava/sandbox (transclusion) (links | )
- User:Kashmiri/sandbox/Spinal muscular atrophy (transclusion) (links | )
- User:Neilsmith38/sandbox (transclusion) (links | )
- User:BSByrne/Athetoid Cerebral Palsy (transclusion) (links | )
- User:Jmevans1230/sandbox (transclusion) (links | )
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- User:Ehubbard3/aniridia (transclusion) (links | )
- User:SaswatPanda/Osteochondrodystrophia Deformans (transclusion) (links | )
- User:P J McGill/Asymmetric crying facies (transclusion) (links | )
- User:Chris3922/sandbox (transclusion) (links | )
- User:BVervers/sandbox (transclusion) (links | )
- User:Aaronabend/sandbox (transclusion) (links | )
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- User:Bluerasberry/Medical condition classification and resources - horizontal test-1 (transclusion) (links | )
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- User:Dmil3422/Laron Syndrome (transclusion) (links | )
- User:Jbobet830/sandbox (transclusion) (links | )
- User:Lukelahood/Myofibrillar myopathy (transclusion) (links | )
- User:Klundern/sandbox (transclusion) (links | )
- User:HAL333/Parkinson's (transclusion) (links | )
- User talk:Yoninah/Archive 6 (transclusion) (links | )
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- Wikipedia talk:WikiProject Clinical medicine/Archive 4 (transclusion) (links | )
- Wikipedia talk:Featured article candidates/New Forest pony/archive1 (transclusion) (links | )
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- Wikipedia talk:WikiProject Molecular Biology/Molecular and Cell Biology/Archive 6 (transclusion) (links | )
- Template:OMIM (transclusion) (links | )
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