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
01062 MCAHS-2;GPIBD-4 multiple congenital anomalies, hypotonia, seizures syndrome, type 2 (MCAHS-2, glycosylphosphatidylinositol deficiency, type 4 (GPIBD-4)) 300868 - 14 13 PIGA - X-linked recessive
01061 PNH-1 hemoglobinuria, nocturnal, paroxysmal, somatic, type 1 (PNH-1) 300818 - 1 0 PIGA - -
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