All diseases

10 entries on 1 page. Showing entries 1 - 10.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00917 - Oculodentodigital dysplasia, autosomal recessive 257850 AR - - GJA1 - -
00918 - Hallermann-Streiff syndrome 234100 AR - - GJA1 - -
00916 AVSD3 septal defect, atrioventricular, type 3 (AVSD-3) 600309 AD - - GJA1 - -
01728 CMDR dysplasia, craniometaphyseal, autosomal recessive (CMDR) 218400 AR - - GJA1 - -
01324 EKVP1 erythrokeratodermia variabilis et progressiva, type 1 133200 AD;AR 18 18 GJA1, GJB3, GJB4 - -
06703 EKVP3 erythrokeratodermia variabilis et progressiva, type 3 617525 AD - - 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 - - - GJA1 - -
00915 SDTY3 syndactyly, type III (SDTY-3) 186100 AD - - GJA1 - -
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