MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandautosomal genetic disease (MONDO:0000429)
..Starting node
..expandautosomal dominant disease ()

       Child Nodes:
........expandacroosteolysis dominant type ()
........expandADULT syndrome ()
........expandamelogenesis imperfecta type 1B ()
........expandautosomal dominant Aarskog syndrome ()
........expandautosomal dominant Alport syndrome ()
........expandautosomal dominant brachyolmia ()
........expandautosomal dominant centronuclear myopathy ()
........expandautosomal dominant chondrodysplasia punctata ()
........expandautosomal dominant deafness - onychodystrophy syndrome ()
........expandautosomal dominant distal renal tubular acidosis ()
........expandautosomal dominant Ehlers-Danlos syndrome, vascular type ()
........expandautosomal dominant ichthyosis vulgaris ()
........expandautosomal dominant Kenny-Caffey syndrome ()
........expandautosomal dominant keratitis ()
........expandautosomal dominant multiple pterygium syndrome ()
........expandautosomal dominant myoglobinuria ()
........expandautosomal dominant omodysplasia ()
........expandautosomal dominant Opitz G/BBB syndrome ()
........expandautosomal dominant polycystic kidney disease ()
........expandautosomal dominant popliteal pterygium syndrome ()
........expandautosomal dominant primary microcephaly ()
........expandautosomal dominant progressive external ophthalmoplegia ()
........expandautosomal dominant Robinow syndrome ()
........expandautosomal dominant sideroblastic anemia ()
........expandautosomal dominant vibratory urticaria ()
........expandBannayan-Riley-Ruvalcaba syndrome ()
........expandBeare-Stevenson cutis gyrata syndrome ()
........expandBirt-Hogg-Dube syndrome ()
........expandblepharo-cheilo-odontic syndrome ()
........expandblepharophimosis, ptosis, and epicanthus inversus syndrome ()
........expandbranchio-oto-renal syndrome ()
........expandbranchiooculofacial syndrome ()
........expandcherubism ()
........expandcongenital polycystic liver disease ()
........expanddysplastic nevus syndrome ()
........expandEhlers-Danlos syndrome, classic type ()
........expandFrasier syndrome ()
........expandgeneralized juvenile polyposis/juvenile polyposis coli ()
........expandhand-foot-genital syndrome ()
........expandhereditary breast ovarian cancer syndrome ()
........expandHolt-Oram syndrome ()
........expandHyper-IgE recurrent infection syndrome 1 ()
........expandLADD syndrome ()
........expandLarsen syndrome ()
........expandLynch syndrome ()
........expandMarfan syndrome ()
........expandmonilethrix ()
........expandMuckle-Wells syndrome ()
........expandmultiple endocrine neoplasia type 1 ()
........expandmultiple endocrine neoplasia type 2B ()
........expandnail-patella syndrome ()
........expandnevoid basal cell carcinoma syndrome ()
........expandNoonan syndrome with multiple lentigines ()
........expandPelger-Huet anomaly ()
........expandpiebaldism ()
........expandproximal symphalangism (disease) ()
........expandRapp-Hodgkin syndrome ()
........expandrenal coloboma syndrome ()
........expandretinoschisis, autosomal dominant ()
........expandspondyloepiphyseal dysplasia tarda, autosomal dominant ()
........expandtarsal-carpal coalition syndrome ()
........expandTownes-Brocks syndrome ()
........expandTreacher-Collins syndrome ()
........expandtrichorhinophalangeal syndrome type I ()
........expandtrichorhinophalangeal syndrome type II ()
........expandtuberous sclerosis ()



 Sister Nodes: 
..expandautosomal dominant disease ()
..expandautosomal recessive disease ()
..expandbrachydactyly-syndactyly syndrome ()
..expandcamptodactyly-tall stature-scoliosis-hearing loss syndrome ()
..expandcongenital factor XI deficiency ()
..expandcongenital factor XII deficiency ()
..expandseptooptic dysplasia ()
..expandWeill-Marchesani syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:426
Name:autosomal dominant disease
Definition:Autosomal dominant form of disease.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:autosomal dominant disease or disorder; autosomal dominant hereditary disorder; autosomal dominant inherited disorder; disease or disorder, autosomal dominant; disease, autosomal dominant
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal