ODCs

Click node...

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Porokeratotic eccrine ostial and dermal duct nevus

X-linked progressive cerebellar ataxia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GJB2	(0.62)	GJB1

Citations in the biomedical literature:

Porokeratotic eccrine ostial and dermal duct nevus		X-linked progressive cerebellar ataxia
	Synonym(s): - Comedo nevus of the palm - Porokeratotic eccrine nevus		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): - Diseases of the nervous system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: x-linked recessive

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

No signs/symptoms info available.