All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01848 CPSID carbamoylphosphate synthetase I deficiency 237300 AR 238 94 CPS1 - -
03913 PHN hypertension, pulmonary, neonatal, susceptibility to (PHN) 615371 - 2 2 CPS1 - -
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