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
03926 MCAHS-3;GPIBD-7 multiple congenital anomalies, hypotonia, seizures syndrome, type 3 (MCAHS-3, glycosylphosphatidylinositol deficiency, type 7 (GPIBD-7)) 615398 - 2 2 PIGT - autosomal recessive
03927 PNH-2 hemoglobinuria, nocturnal, paroxysmal, type 2 (PNH-2) 615399 - 1 1 PIGT - -
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