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17q11 microdeletion syndrome
1 OMIM reference -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
17q11 microdeletion syndrome
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

NF1
(UniProt - OMIM)
 APP
(UniProt - OMIM)
RNF135
(UniProt - OMIM)
SUZ12
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NF1
(0.73)
APP


Citations in the biomedical literature:


17q11 microdeletion syndrome
NF1 RNF135 SUZ12
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



17q11 microdeletion syndrome
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- Del(17)(q11)
- Monosomy 17q11
- NF1 microdeletion syndrome
- Neurofibromatosis type 1 microdeletion syndrome
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
- Rare oncologic disease
- Rare renal disease
- Rare skin disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.