ODCs

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

COMMON GENES: 1

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

Extraskeletal myxoid chondrosarcoma

Hereditary motor and sensory neuropathy, Okinawa type

Citations in the biomedical literature:

Extraskeletal myxoid chondrosarcoma		Hereditary motor and sensory neuropathy, Okinawa type
	Synonym(s): (no synonyms)		Synonym(s): - HMSNP - Hereditary motor and sensory neuropathy, proximal type

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

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: adulthood Average age of death: adult Type of inheritance: sporadic		Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C535717

No signs/symptoms info available.