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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
3 associated genes
No signs/symptoms info
Recessive hereditary methemoglobinemia type 1
Autosomal thrombocytopenia with normal platelets

CYB5R3 ANKRD26
CYCS
MASTL


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CYB5R3
(0.62)
CYCS



Citations in the biomedical literature:


Recessive hereditary methemoglobinemia type 1
CYB5R3
Autosomal thrombocytopenia with normal platelets
ANKRD26 CYCS MASTL



Recessive hereditary methemoglobinemia type 1
Autosomal thrombocytopenia with normal platelets

Synonym(s):
- NADH-cytochrome b5reductase deficiency type 1
- NADH-diaphorase deficiency type 1
- Recessive congenital methemoglobinemia type 1

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
3 OMIM references -
No MeSH references

No signs/symptoms info available.