ODCs

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

PROTEIN INTERACTIONS: 1

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

Pilomatrixoma

Fuchs endothelial corneal dystrophy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CTNNB1	(0.9)	TCF4

Citations in the biomedical literature:

Pilomatrixoma		Fuchs endothelial corneal dystrophy
	Synonym(s): - Epithelioma calcificans of Malherbe - Pilomatricoma		Synonym(s): - Endoepithelial corneal dystrophy - FECD - Late hereditary endothelial dystrophy

	Classification (Orphanet): - Rare oncologic disease - Rare skin disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: D018296		External references: 8 OMIM references - No MeSH references

No signs/symptoms info available.