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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
6 associated genes
No signs/symptoms info
CLN11 disease
Progressive non-fluent aphasia

GRN C9ORF72
CHMP2B
GRN
MAPT
PSEN1
VCP


COMMON
GENES
GRN



Citations in the biomedical literature:


CLN11 disease
GRN
Progressive non-fluent aphasia
C9ORF72 CHMP2B MAPT PSEN1 VCP



CLN11 disease
Progressive non-fluent aphasia

Synonym(s):
(no synonyms)

Synonym(s):
- Agramatic variant of PPA
- Agramatic variant of primary progressive aphasia
- Non-fluent variant PPA

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D057178

No signs/symptoms info available.