All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01771 - Enterokinase deficiency 226200 - - - TMPRSS15 - -
03529 - Trypsinogen deficiency 614044 - - - PRSS1 - -
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 - -
01093 MRT-1 mental retardation, autosomal recessive, type 1 (MRT-1) 249500 - - - PRSS12 - -
00130 PCTT pancreatitis (PCTT) 167800 - - - CFTR, CTRC, PRSS1, SPINK1 - -
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