Progressive non-fluent aphasia |
Lissencephaly due to TUBA1A mutation |
C9ORF72 | TUBA1A | |||
CHMP2B | ||||
GRN | ||||
MAPT | ||||
PSEN1 | ||||
VCP |
INTERACTOME ASSOCIATIONS (click on a score value to see the evidence) |
MAPT | (0.63) | TUBA1A | |
Citations in the biomedical literature:
Progressive non-fluent aphasia |
Lissencephaly due to TUBA1A mutation |
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Synonym(s): - Agramatic variant of PPA- Agramatic variant of primary progressive aphasia - Non-fluent variant PPA | Synonym(s): (no synonyms) | ||
Classification (Orphanet): - Rare genetic disease - Rare neurologic disease | Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease | ||
Classification (ICD10): - Diseases of the nervous system -
| Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -
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Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: adulthood Average age of death: - Type of inheritance: multigenic/multifactorial | Epidemiological data: (no data available)
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External references: 1 OMIM reference -
1 MeSH reference: D057178 | External references: 1 OMIM reference - No MeSH references | ||