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Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

COL4A1
(UniProt - OMIM)
 APP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
COL4A1
(0.52)
APP


Citations in the biomedical literature:


Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures
COL4A1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- HANAC syndrome
- Hereditary angiopathy-nephropathy-aneurysms-muscle cramps syndrome
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: no data available
Type of inheritance: autosomal dominant
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.