ODCs

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8 OMIM references -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Fuchs endothelial corneal dystrophy

Zollinger-Ellison syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TCF4	(0.68)	MEN1

Citations in the biomedical literature:

Fuchs endothelial corneal dystrophy		Zollinger-Ellison syndrome
	Synonym(s): - Endoepithelial corneal dystrophy - FECD - Late hereditary endothelial dystrophy		Synonym(s): - Gastrinoma

	Classification (Orphanet): - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare endocrine disease - Rare gastroenterologic disease - Rare oncologic disease

	Classification (ICD10): - Diseases of the eye and adnexa -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: adulthood Average age of death: normal Type of inheritance: sporadic

	External references: 8 OMIM references - No MeSH references		External references: No OMIM references 2 MeSH references: D015043 / D015408

No signs/symptoms info available.