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Tay-Sachs disease, B variant, infantile form
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Tay-Sachs disease, B variant, juvenile form
1 associated gene
No signs/symptoms info
Tay-Sachs disease, B variant, infantile form
Tay-Sachs disease, B variant, juvenile form

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

COMMON
GENES 		HEXA


Citations in the biomedical literature:


Tay-Sachs disease, B variant, infantile form
HEXA
Tay-Sachs disease, B variant, juvenile form



Tay-Sachs disease, B variant, infantile form
Tay-Sachs disease, B variant, juvenile form

Synonym(s):
- GM2-gangliosidosis, B variant, infantile form
- Hexosaminidase A deficiency, infantile form
Synonym(s):
- GM2-gangliosidosis, B variant, juvenile form
- Hexosaminidase A deficiency, juvenile form
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:
No OMIM references
No MeSH references
No signs/symptoms info available.