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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Familial dementia, British type
Familial dementia, Danish type

ITM2B ITM2B


COMMON
GENES
ITM2B



Citations in the biomedical literature:


Familial dementia, British type
ITM2B
Familial dementia, Danish type



Familial dementia, British type
Familial dementia, Danish type

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
1 MeSH reference: C538208
External references:
1 OMIM reference -
1 MeSH reference: C538209

No signs/symptoms info available.