ODCs

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

PROTEIN INTERACTIONS: 2

1 OMIM reference -
2 associated genes
4 signs/symptoms

Meesmann corneal dystrophy

Localized epidermolysis bullosa simplex

KRT12	(UniProt - OMIM)		KRT14	(UniProt - OMIM)
KRT3	(UniProt - OMIM)		KRT5	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KRT3 KRT3	(0.49) (0.49)	KRT14 KRT5

Citations in the biomedical literature:

Meesmann corneal dystrophy		Localized epidermolysis bullosa simplex
	Synonym(s): - Juvenile hereditary epithelial dystrophy of Meesmann - MECD		Synonym(s): - EBS-loc - Epidermolysis bullosa simplex of palms and soles - Epidermolysis bullosa simplex, Weber-Cockayne type

	Classification (Orphanet): - Rare eye disease - Rare genetic disease		Classification (Orphanet): - 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: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: D053559		External references: 1 OMIM reference - No MeSH references

Localized epidermolysis bullosa simplex
	Very frequent - Autosomal dominant inheritance - Ecchymoses - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment Frequent - Hyperhidrosis / increased sweating
Meesmann corneal dystrophy
(no data available)