ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Hereditary sensorimotor neuropathy with hyperelastic skin

Dentatorubral pallidoluysian atrophy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FBLN5	(0.63)	ATN1

Citations in the biomedical literature:

Hereditary sensorimotor neuropathy with hyperelastic skin		Dentatorubral pallidoluysian atrophy
	Synonym(s): (no synonyms)		Synonym(s): - DRPLA - Dentatorubropallidoluysian atrophy - Naito-Oyanagi disease

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.