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Tay-Sachs disease, B variant, infantile form
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
GM2-gangliosidosis, AB variant
1 OMIM reference -
1 associated gene
No signs/symptoms info
Tay-Sachs disease, B variant, infantile form
GM2-gangliosidosis, AB variant

HEXA
(UniProt - OMIM)
 GM2A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HEXA
(0.68)
GM2A


Citations in the biomedical literature:


Tay-Sachs disease, B variant, infantile form
HEXA
GM2-gangliosidosis, AB variant
GM2A



Tay-Sachs disease, B variant, infantile form
GM2-gangliosidosis, AB variant

Synonym(s):
- GM2-gangliosidosis, B variant, infantile form
- Hexosaminidase A deficiency, infantile form
Synonym(s):
- Hexosaminidase activator deficiency
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.