ODCs

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

PROTEIN INTERACTIONS: 1

2 OMIM references -
1 associated gene
No signs/symptoms info

Familial vascular leukoencephalopathy

Lattice corneal dystrophy type I


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

Citations in the biomedical literature:

Familial vascular leukoencephalopathy		Lattice corneal dystrophy type I
	Synonym(s): - Brain small vessel disease with hemorrhage - Retinal arteriolar tortuosity - infantile hemiparesis - autosomal dominant leukoencephalopathy		Synonym(s): - Biber-Haab-Dimmer dystrophy - Classic lattice corneal dystrophy - LCD1 - LCDI - Lattice corneal dystrophy type 1

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

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

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: C531642		External references: 2 OMIM references - No MeSH references

No signs/symptoms info available.