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

White sponge nevus

Early-onset progressive neurodegeneration - blindness - ataxia - spasticity

KRT13	(UniProt - OMIM)		UCHL1	(UniProt - OMIM)
KRT4	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KRT4	(0.76)	UCHL1

Citations in the biomedical literature:

White sponge nevus		Early-onset progressive neurodegeneration - blindness - ataxia - spasticity
	Synonym(s): - Hereditary mucosal leukokeratosis - White sponge nevus of Cannon		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.