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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
Ménière disease
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures
Ménière disease

COL4A1
(UniProt - OMIM)
 COCH
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
COL4A1
(0.72)
COCH


Citations in the biomedical literature:


Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures
COL4A1
Ménière disease
COCH



Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures
Ménière disease

Synonym(s):
- HANAC syndrome
- Hereditary angiopathy-nephropathy-aneurysms-muscle cramps syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare renal disease
Classification (Orphanet):
- Rare otorhinolaryngologic disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Classification (ICD10):
- Diseases of the ear and mastoid process -
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:
Class of prevalence: 1-5 / 10 000
Average age onset: variable
Average age of death: normal
Type of inheritance: multigenic/multifactorial
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D008575
No signs/symptoms info available.