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Alpha-crystallinopathy
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Autosomal dominant methemoglobinemia
3 associated genes
No signs/symptoms info
Alpha-crystallinopathy
Autosomal dominant methemoglobinemia

CRYAB
(UniProt - OMIM)
 HBA1
(UniProt - OMIM)
HBA2
(UniProt - OMIM)
HBB
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CRYAB
CRYAB
(0.56)
(0.56)
HBA1
HBA2


Citations in the biomedical literature:


Alpha-crystallinopathy
CRYAB
Autosomal dominant methemoglobinemia
HBA1 HBA2 HBB



Alpha-crystallinopathy
Autosomal dominant methemoglobinemia

Synonym(s):
- CRYAB-related myofobrillar myopathy
Synonym(s):
- Hemoglobin M disease
- Hereditary methemoglobinemia due to hemoglobin mutation
- M hemoglobinopathy
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.