ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures

Familial vascular leukoencephalopathy

Citations in the biomedical literature:

Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures		Familial vascular leukoencephalopathy
	Synonym(s): - HANAC syndrome - Hereditary angiopathy-nephropathy-aneurysms-muscle cramps syndrome		Synonym(s): - Brain small vessel disease with hemorrhage - Retinal arteriolar tortuosity - infantile hemiparesis - autosomal dominant leukoencephalopathy

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease - Rare renal disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the eye and adnexa -		Classification (ICD10): - Diseases of the circulatory system -

	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: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C531642

No signs/symptoms info available.