Pages that link to "Template:OMIM"
Jump to navigation
Jump to search
The following pages link to Template:OMIM:
Displayed 250 items.
- Pachydermoperiostosis (transclusion) (← links)
- Hypouricemia (transclusion) (← links)
- Cystinosis (transclusion) (← links)
- Hemopexin (transclusion) (← links)
- HLA-B27 (transclusion) (← links)
- Myoglobin (transclusion) (← links)
- Thiamine (transclusion) (← links)
- Follicle-stimulating hormone (transclusion) (← links)
- Congenital Absence of the Vas Deferens (transclusion) (← links)
- Von Hippel-Lindau disease (transclusion) (← links)
- 5q- syndrome (transclusion) (← links)
- Ectrodactyly (transclusion) (← links)
- Krause-Kivlin syndrome (transclusion) (← links)
- Larsen syndrome (transclusion) (← links)
- Oguchi disease (transclusion) (← links)
- Wallis Zieff Goldblatt syndrome (transclusion) (← links)
- Kindler syndrome (transclusion) (← links)
- Howel-Evans syndrome (transclusion) (← links)
- AREDYLD (transclusion) (← links)
- Young's syndrome (transclusion) (← links)
- Activated protein C resistance (transclusion) (← links)
- Adams Nance syndrome (transclusion) (← links)
- Adenylosuccinate lyase deficiency (transclusion) (← links)
- Aniridia (transclusion) (← links)
- Ataxia telangiectasia (transclusion) (← links)
- Ayazi syndrome (transclusion) (← links)
- Leber's congenital amaurosis (transclusion) (← links)
- Retinitis pigmentosa (transclusion) (← links)
- Bare lymphocyte syndrome (transclusion) (← links)
- Blue diaper syndrome (transclusion) (← links)
- DAB1 (transclusion) (← links)
- Tachykinin peptides (transclusion) (← links)
- Brain-derived neurotrophic factor (transclusion) (← links)
- Ribosomal s6 kinase (transclusion) (← links)
- TCF7L2 (transclusion) (← links)
- Fas ligand (transclusion) (← links)
- Lamin B receptor (transclusion) (← links)
- VLDL receptor (transclusion) (← links)
- RET proto-oncogene (transclusion) (← links)
- MEF2A (transclusion) (← links)
- Autosomal dominant hypophosphatemic rickets (transclusion) (← links)
- Amyloid beta (transclusion) (← links)
- Apolipoprotein E (transclusion) (← links)
- Tylosis (transclusion) (← links)
- Iron overload disorder (transclusion) (← links)
- Hereditary hemorrhagic telangiectasia (transclusion) (← links)
- Phenylthiocarbamide (transclusion) (← links)
- Krüppel (transclusion) (← links)
- Cleft chin (transclusion) (← links)
- Blood type (transclusion) (← links)
- Kell antigen system (transclusion) (← links)
- Kidd antigen system (transclusion) (← links)
- Colton antigen system (transclusion) (← links)
- Yt antigen system (transclusion) (← links)
- Plasmin (transclusion) (← links)
- Tissue factor pathway inhibitor (transclusion) (← links)
- Tissue factor (transclusion) (← links)
- African iron overload (transclusion) (← links)
- McLeod syndrome (transclusion) (← links)
- HLA-B (transclusion) (← links)
- Cenani Lenz syndactylism (transclusion) (← links)
- Congenital afibrinogenemia (transclusion) (← links)
- 2-Hydroxyglutaricaciduria (transclusion) (← links)
- 3 hydroxyisobutyric aciduria (transclusion) (← links)
- 3 methylcrotonic aciduria (transclusion) (← links)
- 6-Pyruvoyltetrahydropterin synthase deficiency (transclusion) (← links)
- Carpenter syndrome (transclusion) (← links)
- Citrullinemia (transclusion) (← links)
- Cockayne syndrome (transclusion) (← links)
- Crouzonodermoskeletal syndrome (transclusion) (← links)
- Dihydropyrimidine dehydrogenase deficiency (transclusion) (← links)
- GAPO syndrome (transclusion) (← links)
- Maple syrup urine disease (transclusion) (← links)
- Mucopolysaccharidosis (transclusion) (← links)
- Ornithine translocase deficiency (transclusion) (← links)
- Periodic paralysis (transclusion) (← links)
- Philadelphia chromosome (transclusion) (← links)
- Photic sneeze reflex (transclusion) (← links)
- Recessive multiple epiphyseal dysplasia (transclusion) (← links)
- SADDAN (transclusion) (← links)
- Sarcosinemia (transclusion) (← links)
- Turcot syndrome (transclusion) (← links)
- Variegate porphyria (transclusion) (← links)
- WAGR syndrome (transclusion) (← links)
- Weissenbacher-Zweymüller syndrome (transclusion) (← links)
- X-linked ichthyosis (transclusion) (← links)
- ZAP70 deficiency (transclusion) (← links)
- Epigenetics (transclusion) (← links)
- PGL2 (transclusion) (← links)
- Abl gene (transclusion) (← links)
- Microcephalin (transclusion) (← links)
- COL1A1 (transclusion) (← links)
- CFTR (gene) (transclusion) (← links)
- HD (gene) (transclusion) (← links)
- MUTYH (transclusion) (← links)
- TBX1 (transclusion) (← links)
- PPOX (transclusion) (← links)
- IKBKAP (transclusion) (← links)
- Pax genes (transclusion) (← links)
- 3-hydroxy-3-methylglutaryl-CoA lyase (transclusion) (← links)
- LMNA (transclusion) (← links)
- UDP galactose epimerase (transclusion) (← links)
- Titin (transclusion) (← links)
- Ataxin 7 (transclusion) (← links)
- Thrombopoietin (transclusion) (← links)
- Superoxide dismutase (transclusion) (← links)
- Huntingtin (transclusion) (← links)
- Electron-transferring-flavoprotein dehydrogenase (transclusion) (← links)
- SLC26A2 (transclusion) (← links)
- Myelin oligodendrocyte glycoprotein (transclusion) (← links)
- COL11A2 (transclusion) (← links)
- VPS13B (transclusion) (← links)
- ADAMTS13 (transclusion) (← links)
- Abelson leukemia virus protein (transclusion) (← links)
- Fukutin (transclusion) (← links)
- Mannan-binding lectin (transclusion) (← links)
- Lactate dehydrogenase (transclusion) (← links)
- Mevalonate kinase (transclusion) (← links)
- N-acetylglucosamine-1-phosphate transferase (transclusion) (← links)
- ETV6 (transclusion) (← links)
- Fumarylacetoacetate hydrolase (transclusion) (← links)
- Glial fibrillary acidic protein (transclusion) (← links)
- Wiskott-Aldrich syndrome protein (transclusion) (← links)
- OCRL (transclusion) (← links)
- Monoamine oxidase A (transclusion) (← links)
- Acetylserotonin O-methyltransferase (transclusion) (← links)
- Doublecortin (transclusion) (← links)
- Fatal familial insomnia (transclusion) (← links)
- Hyper IgM Syndrome Type 5 (transclusion) (← links)
- Wikipedia:WikiProject Molecular and Cellular Biology/Style guidelines (transclusion) (← links)
- Lucey-Driscoll syndrome (transclusion) (← links)
- Hyperpipecolatemia (transclusion) (← links)
- Pyruvate kinase (transclusion) (← links)
- Fissured tongue (transclusion) (← links)
- Phosphate-regulating endopeptidase gene (transclusion) (← links)
- Nodal (protein) (transclusion) (← links)
- Troponin C (transclusion) (← links)
- TRPV4 (transclusion) (← links)
- BACE2 (transclusion) (← links)
- Tuftsin (transclusion) (← links)
- Xanthine oxidase (transclusion) (← links)
- Bone morphogenetic protein 4 (transclusion) (← links)
- Rab (G-protein) (transclusion) (← links)
- Cytochrome C1 (transclusion) (← links)
- Adiposis dolorosa (transclusion) (← links)
- Adrenocorticotropic hormone deficiency (transclusion) (← links)
- Cystic medial necrosis (transclusion) (← links)
- Familial male precocious puberty (transclusion) (← links)
- Fountain syndrome (transclusion) (← links)
- Glucocorticoid deficiency 1 (transclusion) (← links)
- Hypertrichosis lanuginosa (transclusion) (← links)
- Male pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase deficiency (transclusion) (← links)
- Methylmalonic acidemia (transclusion) (← links)
- Pacman dysplasia (transclusion) (← links)
- Zaspopathy (transclusion) (← links)
- Hereditary spherocytosis (transclusion) (← links)
- Congenital absence of the vas deferens (transclusion) (← links)
- Zori Stalker Williams syndrome (transclusion) (← links)
- Freeman-Sheldon syndrome (transclusion) (← links)
- Hyperammonemia (transclusion) (← links)
- Spermatogenesis arrest (transclusion) (← links)
- ICF syndrome (transclusion) (← links)
- Meleda Disease (transclusion) (← links)
- Michelin tire baby syndrome (transclusion) (← links)
- Mullerian agenesis (transclusion) (← links)
- Pachygyria (transclusion) (← links)
- Pentalogy of Cantrell (transclusion) (← links)
- Progressive supranuclear palsy (transclusion) (← links)
- Mevalonic aciduria (transclusion) (← links)
- Methylmalonyl-CoA mutase deficiency (transclusion) (← links)
- Neuronal ceroid lipofuscinosis (transclusion) (← links)
- HEC syndrome (transclusion) (← links)
- Donohue syndrome (transclusion) (← links)
- Monosomy 9p (transclusion) (← links)
- Nezelof syndrome (transclusion) (← links)
- Grey platelet syndrome (transclusion) (← links)
- Patterson syndrome (transclusion) (← links)
- Da Costa's syndrome (transclusion) (← links)
- Hyper IgM Syndrome Type 2 (transclusion) (← links)
- Melanocortin 1 receptor (transclusion) (← links)
- CD244 (transclusion) (← links)
- Phosphoinositide 3-kinase (transclusion) (← links)
- C-Raf (transclusion) (← links)
- Neuregulin (transclusion) (← links)
- Hedgehog signaling pathway (transclusion) (← links)
- H19 (gene) (transclusion) (← links)
- Branchio-oto-renal syndrome (transclusion) (← links)
- PACS1 (transclusion) (← links)
- TFAP2A (transclusion) (← links)
- RIPK1 (transclusion) (← links)
- Sequestosome 1 (transclusion) (← links)
- Interferon gamma receptor 1 (transclusion) (← links)
- NT5E (transclusion) (← links)
- SAT1 (gene) (transclusion) (← links)
- KCNJ5 (transclusion) (← links)
- SLC25A3 (transclusion) (← links)
- Thiamin (transclusion) (← links)
- Antley-Bixler syndrome (transclusion) (← links)
- MEF2C (transclusion) (← links)
- Rothmund-Thomson syndrome (transclusion) (← links)
- SLC25A10 (transclusion) (← links)
- Brunner syndrome (transclusion) (← links)
- Potassium cyanide (transclusion) (← links)
- Cytochrome b5 (transclusion) (← links)
- Freckles (transclusion) (← links)
- Carnosinemia (transclusion) (← links)
- Jansky-Bielschowsky disease (transclusion) (← links)
- CD79A (transclusion) (← links)
- Gunther disease (transclusion) (← links)
- Argininemia (transclusion) (← links)
- Acrocephalosyndactylia (transclusion) (← links)
- Hyper-IgM syndrome type 2 (transclusion) (← links)
- Hyper-IgM syndrome type 5 (transclusion) (← links)
- Beta amyloid (transclusion) (← links)
- LAMP2 (transclusion) (← links)
- Timeline of tuberous sclerosis (transclusion) (← links)
- Beta-mannosidosis (transclusion) (← links)
- Fibrochondrogenesis (transclusion) (← links)
- Hexokinase deficiency (transclusion) (← links)
- HK1 (transclusion) (← links)
- Acrocallosal syndrome (transclusion) (← links)
- Ichthyosis bullosa of Siemens (transclusion) (← links)
- Hypoplastic left heart syndrome causes (transclusion) (← links)
- Hereditary nonpolyposis colorectal cancer pathophysiology (transclusion) (← links)
- Geroderma osteodysplastica (transclusion) (← links)
- Aplasia cutis congenita (transclusion) (← links)
- Lawrence-Moon syndrome (transclusion) (← links)
- Achalasia-addisonian syndrome (transclusion) (← links)
- Galactose epimerase deficiency (transclusion) (← links)
- Arthrogryposis classification (transclusion) (← links)
- Gaucher's disease pathophysiology (transclusion) (← links)
- Ataxia telangiectasia pathophysiology (transclusion) (← links)
- Thalassemia pathophysiology (transclusion) (← links)
- Maturity onset diabetes of the young pathophysiology (transclusion) (← links)
- Nephrogenic diabetes insipidus causes (transclusion) (← links)
- Papillorenal syndrome overview (transclusion) (← links)
- Potter syndrome classification (transclusion) (← links)
- Retinitis causes (transclusion) (← links)
- Dyskeratosis congenita overview (transclusion) (← links)
- Buschke–Ollendorff syndrome (transclusion) (← links)
- Schindler disease (transclusion) (← links)
- 2-methylbutyryl-coenzyme a dehydrogenase deficiency (transclusion) (← links)
- Hypertryptophanemia (transclusion) (← links)
- WARG syndrome (transclusion) (← links)
- Basement membrane corneal dystrophy (transclusion) (← links)
- Pontocerebellar hypoplasia (transclusion) (← links)
- Permanent neonatal diabetes mellitus (transclusion) (← links)
- Microvillus inclusion disease (transclusion) (← links)
- Transthyretin-related hereditary amyloidosis (transclusion) (← links)
- Sandbox: HTM (transclusion) (← links)