ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
6 signs/symptoms

Meesmann corneal dystrophy

Naegeli-Franceschetti-Jadassohn syndrome

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		Naegeli-Franceschetti-Jadassohn syndrome
	Synonym(s): - Juvenile hereditary epithelial dystrophy of Meesmann - MECD		Synonym(s): - NFJ syndrome - Naegeli syndrome

	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: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant

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

Naegeli-Franceschetti-Jadassohn syndrome
	Very frequent - Autosomal dominant inheritance - Dysplastic / thick / grooved fingernails - Dysplastic / thick / grooved toenails - Enamel anomaly - Irregular / in bands / reticular skin hyperpigmentation - Palmoplantar hyperkeratosis / keratoderma
Meesmann corneal dystrophy
(no data available)