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Tay-Sachs disease, B variant, infantile form
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Non-spherocytic hemolytic anemia due to hexokinase deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Tay-Sachs disease, B variant, infantile form
Non-spherocytic hemolytic anemia due to hexokinase deficiency

HEXA
(UniProt - OMIM)
 HK1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HEXA
(0.63)
HK1


Citations in the biomedical literature:


Tay-Sachs disease, B variant, infantile form
HEXA
Non-spherocytic hemolytic anemia due to hexokinase deficiency
HK1



Tay-Sachs disease, B variant, infantile form
Non-spherocytic hemolytic anemia due to hexokinase deficiency

Synonym(s):
- GM2-gangliosidosis, B variant, infantile form
- Hexosaminidase A deficiency, infantile form
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
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: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.