All diseases

10 entries on 1 page. Showing entries 1 - 10.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00917 - Oculodentodigital dysplasia, autosomal recessive 257850 AR 0 0 GJA1 - -
00918 - Hallermann-Streiff syndrome 234100 AR 0 0 GJA1 - -
00916 AVSD3 septal defect, atrioventricular, type 3 (AVSD-3) 600309 AD 0 0 GJA1 - -
01728 CMDR dysplasia, craniometaphyseal, autosomal recessive (CMDR) 218400 AR 0 0 GJA1 - -
01324 EKVP1 Erythrokeratodermia variabilis et progressiva 1 133200 AD;AR 18 18 GJA1, GJB3, GJB4 - -
06703 EKVP3 Erythrokeratodermia variabilis et progressiva 3 617525 AD 0 0 GJA1 - -
00390 HLHS1 heart, hypoplastic left, syndrome (HLHS) 241550 AR 37 37 GJA1 - -
00914 ODDD Oculodentodigital dysplasia 164200 AD 1 1 GJA1 - -
04486 PPKCA1 keratoderma, palmoplantar, with congenital alopecia, type 1 (PPKCA-1) 104100 - 0 0 GJA1 - -
00915 SDTY3 syndactyly, type III (SDTY-3) 186100 AD 0 0 GJA1 - -
Legend   How to query