ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Meesmann corneal dystrophy

Dermatopathia pigmentosa reticularis

KRT12	(UniProt - OMIM)		KRT14	(UniProt - OMIM)
KRT3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KRT3	(0.49)	KRT14

Citations in the biomedical literature:

Meesmann corneal dystrophy		Dermatopathia pigmentosa reticularis
	Synonym(s): - Juvenile hereditary epithelial dystrophy of Meesmann - MECD		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Diseases of the eye and adnexa -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: D053559		External references: 1 OMIM reference - 1 MeSH reference: C535374

No signs/symptoms info available.