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Paroxysmal nocturnal hemoglobinuria
2 OMIM references -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
West syndrome
2 OMIM references -
6 associated genes
No signs/symptoms info
Paroxysmal nocturnal hemoglobinuria
West syndrome

PIGA
(UniProt - OMIM)
 ARX
(UniProt - OMIM)
CDKL5
(UniProt - OMIM)
GRIN2B
(UniProt - OMIM)
PIGA
(UniProt - OMIM)
SCN2A
(UniProt - OMIM)
ST3GAL3
(UniProt - OMIM)

COMMON
GENES 		PIGA


Citations in the biomedical literature:


Paroxysmal nocturnal hemoglobinuria
PIGA
West syndrome
ARX CDKL5 GRIN2B SCN2A ST3GAL3



Paroxysmal nocturnal hemoglobinuria
West syndrome

Synonym(s):
- Marchiafava-Micheli disease
- PNH
Synonym(s):
- Infantile spasms
- Intellectual deficit - hypsarrhythmia
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
1 MeSH reference: D006457
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.