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Distal 17p13.3 microdeletion syndrome
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Behavioral variant of frontotemporal dementia
1 OMIM reference -
6 associated genes
No signs/symptoms info
Distal 17p13.3 microdeletion syndrome
Behavioral variant of frontotemporal dementia

YWHAE
(UniProt - OMIM)
 C9ORF72
(UniProt - OMIM)
CHMP2B
(UniProt - OMIM)
GRN
(UniProt - OMIM)
MAPT
(UniProt - OMIM)
PSEN1
(UniProt - OMIM)
VCP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
YWHAE
(0.63)
VCP


Citations in the biomedical literature:


Distal 17p13.3 microdeletion syndrome
YWHAE
Behavioral variant of frontotemporal dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP



Distal 17p13.3 microdeletion syndrome
Behavioral variant of frontotemporal dementia

Synonym(s):
- Distal del(17)(p13.3 )
- Distal monosomy 17p13.3
Synonym(s):
- bv-FTD
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.