ODCs

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

PROTEIN INTERACTIONS: 1

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

Lattice corneal dystrophy type I

Familial vascular leukoencephalopathy


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

Citations in the biomedical literature:

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

	Classification (Orphanet): - Rare eye disease - Rare genetic 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: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.