Pages that link to "OMIM"
← OMIM
The following pages link to OMIM:
Displayed 500 items.
- Sarcoidosis (← links)
- Osteopetrosis (← links)
- Tyrosinemia (← links)
- Cystinuria (← links)
- Achalasia (← links)
- Hemochromatosis (← links)
- Narcolepsy (← links)
- Brachydactyly (← links)
- Anencephaly (← links)
- Neuroacanthocytosis (← links)
- Pulmonary valve stenosis (← links)
- Cholinesterase (← links)
- Ferritin (← links)
- Fibrinogen (← links)
- Gamma-glutamyl transpeptidase (← links)
- Hemoglobin (← links)
- Eczema (← links)
- Acromegaly (← links)
- Polydactyly (← links)
- Paroxysmal nocturnal hemoglobinuria (← links)
- Spondylolisthesis (← links)
- Carcinoma (← links)
- Kallman syndrome (← links)
- Atransferrinemia (← links)
- Pentosuria (← links)
- Trimethylaminuria (← links)
- Anisocoria (← links)
- Scurvy (← links)
- Arthrogryposis (← links)
- Mitral valve prolapse (← links)
- Ehlers-Danlos syndrome (← links)
- Protamine (← links)
- Situs inversus (← links)
- Gastroesophageal reflux disease (← links)
- Human chorionic gonadotropin (← links)
- Growth hormone (← links)
- Marfan's syndrome (← links)
- Amyotrophic lateral sclerosis (← links)
- Charcot-Marie-Tooth Syndrome (← links)
- Androgen insensitivity syndrome (← links)
- Macroglossia (← links)
- Sickle-cell disease (← links)
- Follicle-stimulating hormone (← links)
- Luteinizing hormone (← links)
- Pancreatic polypeptide (← links)
- Multiple endocrine neoplasia (← links)
- Adrenocorticotropic hormone (← links)
- Thyrotropin-releasing hormone (← links)
- 22q11.2 deletion syndrome (← links)
- Angelman syndrome (← links)
- Autoimmunity (← links)
- Hemosiderosis (← links)
- Aceruloplasminemia (← links)
- Achondrogenesis (← links)
- Adrenoleukodystrophy (← links)
- Alkaptonuria (← links)
- Craniosynostosis (← links)
- Pfeiffer syndrome (← links)
- Von Hippel-Lindau disease (← links)
- Werner syndrome (← links)
- Krabbe disease (← links)
- Oculopharyngeal muscular dystrophy (← links)
- Farber disease (← links)
- Cholesteryl ester storage disease (← links)
- Fumarase deficiency (← links)
- Alagille syndrome (← links)
- Mulibrey nanism (← links)
- Stickler syndrome (← links)
- Thanatophoric dysplasia (← links)
- Robinow syndrome (← links)
- Epidermolysis bullosa simplex (← links)
- Pallister-Killian syndrome (← links)
- Poland syndrome (← links)
- Acromicric dysplasia (← links)
- Ectrodactyly (← links)
- Lesch-Nyhan's syndrome (← links)
- Kasabach-Merritt syndrome (← links)
- Ichthyosis lamellaris (← links)
- X-linked alpha thalassemia mental retardation syndrome (← links)
- Neonatal hemochromatosis (← links)
- Kabuki syndrome (← links)
- Leukocyte adhesion deficiency (← links)
- Congenital insensitivity to pain (← links)
- Zellweger syndrome (← links)
- Walker-Warburg syndrome (← links)
- Kearns-Sayre syndrome (← links)
- Saethre-Chotzen syndrome (← links)
- Nail-patella syndrome (← links)
- Myoneurogenic gastrointestinal encephalopathy (← links)
- Parry-Romberg syndrome (← links)
- Harlequin type ichthyosis (← links)
- Congenital insensitivity to pain with anhidrosis (← links)
- Larsen syndrome (← links)
- Dupuytrens contracture (← links)
- ABCD syndrome (← links)
- Oguchi disease (← links)
- Occipital horn syndrome (← links)
- Geographic tongue (← links)
- Fitzsimmons-Guilbert syndrome (← links)
- Rabson-Mendenhall syndrome (← links)
- Wallis Zieff Goldblatt syndrome (← links)
- Hallermann-Streiff syndrome (← links)
- Epidermodysplasia verruciformis (← links)
- Epidermolytic hyperkeratosis (← links)
- Chédiak-Higashi syndrome (← links)
- Menkes disease (← links)
- Mowat-Wilson syndrome (← links)
- Fibrodysplasia ossificans progressiva (← links)
- Upington disease (← links)
- Young's syndrome (← links)
- Young Simpson syndrome (← links)
- 3c syndrome (← links)
- Aase syndrome (← links)
- Abdallat Davis Farrage syndrome (← links)
- Ablepharon macrostomia syndrome (← links)
- Achard syndrome (← links)
- Acheiropodia (← links)
- Achromatopsia (← links)
- Acrodysostosis (← links)
- Adenosine deaminase deficiency (← links)
- Adenylosuccinate lyase deficiency (← links)
- Ainhum (← links)
- Albright's hereditary osteodystrophy (← links)
- Aldolase A deficiency (← links)
- Alternating hemiplegia of childhood (← links)
- Aniridia (← links)
- Apert syndrome (← links)
- Apparent mineralocorticoid excess (← links)
- Arakawa's syndrome II (← links)
- Arginemia (← links)
- Argininosuccinic aciduria (← links)
- Arnold-Chiari malformation (← links)
- Arrhythmogenic right ventricular dysplasia (← links)
- Ataxia telangiectasia (← links)
- Hydrogen potassium ATPase (← links)
- Motilin (← links)
- Uroguanylin (← links)
- Accessory breast (← links)
- Bardet-Biedl syndrome (← links)
- Leber's congenital amaurosis (← links)
- Progressive external ophthalmoplegia (← links)
- Aphakia (← links)
- Vitelliform macular dystrophy (← links)
- Keratoconus (← links)
- Choroideremia (← links)
- Blepharophimosis (← links)
- X-linked congenital stationary night blindness (← links)
- Retinitis pigmentosa (← links)
- Leber's hereditary optic neuropathy (← links)
- Bare lymphocyte syndrome (← links)
- Barth syndrome (← links)
- Batten disease (← links)
- Bethlem myopathy (← links)
- Bipolar disorder (← links)
- Biotinidase deficiency (← links)
- Bloom syndrome (← links)
- Lissencephaly (← links)
- Arachnoid cyst (← links)
- Muenke syndrome (← links)
- ASPM (Genetics) (← links)
- Low affinity nerve growth factor receptor (← links)
- BK channel (← links)
- Cation channels of sperm (← links)
- P2X receptor (← links)
- Two-pore channel (← links)
- T-type calcium channel (← links)
- R-type calcium channel (← links)
- Q-type calcium channel (← links)
- P-type calcium channel (← links)
- N-type calcium channel (← links)
- CACNA1C (← links)
- TRPA (channel) (← links)
- Substance P (← links)
- Gastrin releasing peptide (← links)
- Beta-endorphin (← links)
- Cholinesterase enzyme (← links)
- Dynorphin (← links)
- Corticotropin-like intermediate peptide (← links)
- Neuromedin B (← links)
- Orexin (← links)
- Neuromedin U (← links)
- VMAT1 (← links)
- VMAT2 (← links)
- Delta opioid receptor (← links)
- Mu opioid receptor (← links)
- Kappa opioid receptor (← links)
- Glia maturation factor (← links)
- Calcineurin (← links)
- Inositol triphosphate receptor (← links)
- A1 receptor (← links)
- Wnt signaling pathway (← links)
- Casein kinase 1 (← links)
- Casein kinase 2 (← links)
- Frzb (← links)
- Prickle (protein) (← links)
- Extracellular signal-regulated kinases (← links)
- LHRH receptor (← links)
- Hepatocyte nuclear factors (← links)
- Aryl hydrocarbon receptor repressor (← links)
- Rab27 (← links)
- STAT5 (← links)
- Platelet-derived growth factor receptor (← links)
- PHLPP (← links)
- Calsequestrin (← links)
- Interleukin 1 (← links)
- Interleukin 12 (← links)
- Visfatin (← links)
- Interleukin 28 (← links)
- Interleukin 27 (← links)
- Interleukin 14 (← links)
- Interleukin 17 (← links)
- Interleukin 23 (← links)
- CCL28 (← links)
- IL-2 receptor (← links)
- CCL25 (← links)
- CCL13 (← links)
- RANTES (← links)
- CCL14 (← links)
- CCL15 (← links)
- CCL16 (← links)
- CCL1 (← links)
- CCL23 (← links)
- CCL24 (← links)
- CCL26 (← links)
- CCL27 (← links)
- CXCL2 (← links)
- CXCL14 (← links)
- CXC chemokine receptors (← links)
- CC chemokine receptors (← links)
- CXCL6 (← links)
- CXCL16 (← links)
- XCL2 (← links)
- IFNGR (← links)
- Macrophage inflammatory protein (← links)
- Autocrine motility factor (← links)
- Lymphotoxin (← links)
- Protease-activated receptor (← links)
- Low density lipoprotein receptor-related protein 8 (← links)
- Thyroid hormone receptor (← links)
- Peroxisome proliferator-activated receptor (← links)
- Estrogen receptor (← links)
- Retinoid X receptor (← links)
- Liver X receptor (← links)
- Retinoic acid receptor (← links)
- RAR-related orphan receptor (← links)
- Rev-ErbA (← links)
- Testicular receptor (← links)
- Chicken ovalbumin upstream promoter-transcription factor (← links)
- Glycophorin C (← links)
- Ryanodine receptor (← links)
- Neuropilin (← links)
- GABAB receptor (← links)
- TGF beta receptors (← links)
- Cholecystokinin receptor (← links)
- Angiotensin receptor (← links)
- H1 receptor (← links)
- H₂ receptor (← links)
- H₃ receptor (← links)
- H4 receptor (← links)
- Endothelin receptor (← links)
- Cannabinoid receptor (← links)
- Gonadotropin-releasing hormone receptor (← links)
- Bradykinin receptor (← links)
- Parathyroid hormone receptor (← links)
- Neurotensin receptor (← links)
- Somatostatin receptor (← links)
- MC1R (← links)
- Tachykinin receptor (← links)
- Vasopressin receptor (← links)
- Vasoactive intestinal peptide receptor (← links)
- EGF module-containing mucin-like hormone receptor (← links)
- Neuropeptide Y receptor (← links)
- Orexin receptor (← links)
- Neuromedin U receptor (← links)
- TACR1 (← links)
- Prokineticin receptor (← links)
- Free fatty acid receptor (← links)
- SREB (← links)
- Retinoic acid-inducible orphan G protein-coupled receptor (← links)
- Relaxin receptor (← links)
- Flamingo (protein) (← links)
- Angiopoietin Receptors: Tie-1 & Tie-2 (← links)
- Her 3 (← links)
- Her 4 (← links)
- MuSK protein (← links)
- TrkA (← links)
- TrkB (← links)
- TrkC (← links)
- VEGF receptors (← links)
- Hypoxia inducible factors (← links)
- Sox2 (← links)
- Myf5 (← links)
- Myf6 (← links)
- MCEF (← links)
- TFIIA (← links)
- Transcription Factor II D (← links)
- Transcription Factor II H (← links)
- Transcription Factor II E (← links)
- Transcription Factor II F (← links)
- Activating protein 2 (← links)
- Gli2 (← links)
- Gli3 (← links)
- Gli1 (← links)
- Oct-2 (← links)
- 5-alpha-reductase deficiency (← links)
- Nesidioblastosis (← links)
- Kennedy disease (← links)
- Autoimmune polyendocrine syndrome (← links)
- Duane syndrome (← links)
- Arcus senilis (← links)
- Distichia (← links)
- Zonular cataract and nystagmus (← links)
- Amyloid beta (← links)
- APH-1 (← links)
- PEN-2 (← links)
- Orthostatic intolerance (← links)
- Loeys-Dietz syndrome (← links)
- Dubin-Johnson syndrome (← links)
- Acute fatty liver of pregnancy (← links)
- Iron overload disorder (← links)
- Food allergy (← links)
- Shwachman-Diamond syndrome (← links)
- Intestinal pseudoobstruction (← links)
- Hereditary hemorrhagic telangiectasia (← links)
- Ondine's curse (← links)
- Hamman-Rich syndrome (← links)
- Anti-müllerian hormone (← links)
- Thymosin (← links)
- Prokineticin (← links)
- Bradykinin (← links)
- Melanocyte-stimulating hormone (← links)
- Activin (← links)
- Inhibin (← links)
- Obestatin (← links)
- Relaxin (← links)
- Growth hormone releasing hormone (← links)
- Human placental lactogen (← links)
- Hepcidin (← links)
- Agouti signalling peptide (← links)
- Double outlet right ventricle (← links)
- Proinsulin (← links)
- Taussig-Bing syndrome (← links)
- Uhl anomaly (← links)
- Amelogenin (← links)
- Angiopoietin (← links)
- XX male syndrome (← links)
- EBP (gene) (← links)
- Scleraxis (← links)
- MASS phenotype (← links)
- Complement component 4 (← links)
- Decay accelerating factor (← links)
- Band 3 (← links)
- XK (protein) (← links)
- Kell antigen system (← links)
- Human serum albumin (← links)
- Fibrin (← links)
- Fetuin (← links)
- Alpha 2-macroglobulin (← links)
- Serum amyloid A (← links)
- Orosomucoid (← links)
- C1Q complex (← links)
- C3 (complement) (← links)
- C5a (← links)
- C8 complex (← links)
- Complement component 1R (← links)
- Complement component 1S (← links)
- Complement component 7 (← links)
- Complement component 9 (← links)
- Apolipoprotein A2 (← links)
- Protein Z-related protease inhibitor (← links)
- Protein Z (← links)
- Factor XIII (← links)
- Thrombin-activatable fibrinolysis inhibitor (← links)
- Hemolytic-uremic syndrome (← links)
- X-linked agammaglobulinemia (← links)
- Polycystic liver disease (← links)
- Single nucleotide polymorphism (← links)
- HLA-DQ8 (← links)
- HLA-DQ4 (← links)
- Omphalocele (← links)
- Septo-optic dysplasia (← links)
- Imperforate anus (← links)
- Agenesis of the corpus callosum (← links)
- Goldenhar syndrome (← links)
- Prune belly syndrome (← links)
- Holoprosencephaly (← links)
- Porencephaly (← links)
- Schizencephaly (← links)
- Variome (← links)
- DNA clamp (← links)
- 17-beta-hydroxysteroid dehydrogenase deficiency (← links)
- 22q13 deletion syndrome (← links)
- 3-Methylglutaconic aciduria (← links)
- 3-hydroxy-3-methylglutaryl-CoA lyase deficiency (← links)
- 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (← links)
- ALA dehydratase deficiency (← links)
- Adducted thumb syndrome (← links)
- Asperger syndrome (← links)
- Autosomal dominant nocturnal frontal lobe epilepsy (← links)
- Bartter syndrome (← links)
- Beckwith-Wiedemann syndrome (← links)
- Benign familial neonatal convulsions (← links)
- Beta-ketothiolase deficiency (← links)
- Birt-Hogg-Dubé syndrome (← links)
- CADASIL (← links)
- Canavan disease (← links)
- Carbamoyl phosphate synthetase I deficiency (← links)
- Cardiofaciocutaneous syndrome (← links)
- Carnitine palmitoyltransferase I deficiency (← links)
- Carnitine palmitoyltransferase II deficiency (← links)
- Carpenter syndrome (← links)
- Chronic granulomatous disease (← links)
- Citrullinemia (← links)
- Coffin-Lowry syndrome (← links)
- Cohen syndrome (← links)
- Congenital disorder of glycosylation (← links)
- Cornelia de Lange Syndrome (← links)
- Costello syndrome (← links)
- Crouzon syndrome (← links)
- Darier's disease (← links)
- Dejerine Sottas syndrome (← links)
- Diamond-Blackfan anemia (← links)
- Diastrophic dysplasia (← links)
- Duane-radial ray syndrome (← links)
- Dubowitz syndrome (← links)
- Duchenne muscular dystrophy (← links)
- Ellis-van Creveld syndrome (← links)
- Emery-Dreifuss muscular dystrophy (← links)
- Essential fructosuria (← links)
- Facioscapulohumeral muscular dystrophy (← links)
- Familial atrial fibrillation (← links)
- Familial hemiplegic migraine (← links)
- Feingold syndrome (← links)
- Fragile X syndrome (← links)
- Friedreich's ataxia (← links)
- Fructose malabsorption (← links)
- Galactose-1-phosphate uridylyltransferase galactosemia (← links)
- Gardner's syndrome (← links)
- Generalized epilepsy with febrile seizures plus (← links)
- Gitelman syndrome (← links)
- Glucose-galactose malabsorption (← links)
- Glutathione synthetase deficiency (← links)
- Greig cephalopolysyndactyly syndrome (← links)
- Guanidinoacetate methyltransferase deficiency (← links)
- Hereditary coproporphyria (← links)
- Hereditary multiple exostoses (← links)
- Histidinemia (← links)
- Holocarboxylase synthetase deficiency (← links)
- Holt-Oram syndrome (← links)
- Huntington's disease (← links)
- Hyper-IgE syndrome (← links)
- Hyperkalemic periodic paralysis (← links)
- Hyperlysinemia (← links)
- Hyperprolinemia (← links)
- Hypochondroplasia (← links)
- Hypokalemic periodic paralysis (← links)
- Hypomagnesemia with secondary hypocalcemia (← links)
- Ichthyosis vulgaris (← links)
- Infantile cortical hyperostosis (← links)
- Infantile neuroaxonal dystrophy (← links)
- Isobutyryl-coenzyme A dehydrogenase deficiency (← links)
- Jackson-Weiss syndrome (← links)
- Jacobsen syndrome (← links)
- Juvenile myoclonic epilepsy (← links)
- Kallmann syndrome (← links)
- Kniest dysplasia (← links)
- Langer-Giedion syndrome (← links)
- Laurence-Moon syndrome (← links)
- Li-Fraumeni syndrome (← links)
- Liddle's syndrome (← links)
- Lysinuric protein intolerance (← links)
- Léri-Weill dyschondrosteosis (← links)
- Machado-Joseph disease (← links)
- Malonyl-CoA decarboxylase deficiency (← links)
- Meckel syndrome (← links)
- Medium-chain acyl-coenzyme A dehydrogenase deficiency (← links)
- Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (← links)
- Mitochondrial trifunctional protein deficiency (← links)
- Muscular dystrophy (← links)
- Myeloperoxidase deficiency (← links)
- Myotonia congenita (← links)
- Myotonic dystrophy (← links)
- N-Acetylglutamate synthase deficiency (← links)
- Nemaline myopathy (← links)
- Nephronophthisis (← links)
- Neurofibromatosis type I (← links)
- Neurofibromatosis type II (← links)
- Neuropathy, ataxia, and retinitis pigmentosa (← links)
- Nevoid basal cell carcinoma syndrome (← links)
- Norrie disease (← links)
- Ornithine transcarbamylase deficiency (← links)
- Otospondylomegaepiphyseal dysplasia (← links)
- Paroxysmal extreme pain disorder (← links)
- Pendred syndrome (← links)
- Prader-Willi syndrome (← links)
- Primary carnitine deficiency (← links)
- Primary ciliary dyskinesia (← links)
- Prolidase deficiency (← links)
- Pseudoachondroplasia (← links)
- Pyruvate carboxylase deficiency (← links)