All diseases

4 entries on 1 page. Showing entries 1 - 4.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01771 - Enterokinase deficiency 226200 1 1 TMPRSS15 - -
03529 - Trypsinogen deficiency 614044 0 0 PRSS1 - -
01093 MRT-1 mental retardation, autosomal recessive, type 1 (MRT-1) 249500 0 0 PRSS12 - -
00130 PCTT pancreatitis (PCTT) 167800 3 1 CFTR, CTRC, PRSS1, SPINK1 - -