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Paroxysmal nocturnal hemoglobinuria
2 OMIM references -
1 associated gene
3 connected diseases
No signs/symptoms info
Disease Type of connection
Multiple congenital anomalies-hypotonia-seizures syndrome type 2
West syndrome
Congenital muscular dystrophy with intellectual disability and severe epilepsy
Synonym(s):
- Marchiafava-Micheli disease
- PNH
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
External references:
2 OMIM references -
1 MeSH reference: D006457
Gene symbol UniProt reference OMIM reference
PIGA P37287311770
No signs/symptoms info available.