All diseases

8 entries on 1 page. Showing entries 1 - 8.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00829 - immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia 300853 - - - MAGT1 - -
00963 CDG-1J glycosylation, congenital disorder of, type Ij (CDG-1J) 608093 - - - DPAGT1 - -
00964 CMSTA-2 myasthenic syndrome, congenital, with tubular aggregates, type 2 (CMSTA-2) 614750 - - - DPAGT1 - -
00104 EHT hypertension, essential (EHT) 145500 - - - ADD1, AGT, AGTR1, ATP1B1, CYP3A5, ECE1, GNB3, NOS2, NOS3, PTGIS, RGS5, SELE - -
00139 ID intellectual disability (ID) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
01123 MRX-88 mental retardation, X-linked, type 88 (MRX-88) 300852 - - - AGTR2 - -
00828 MRX-95 mental retardation, X-linked, type 95 (MRX-95) 300716 - - - MAGT1 - -
00254 RTD dysgenesis, renal tubular (RTD) 267430 - - - ACE, AGT, AGTR1, REN - -
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