ODCs

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2 OMIM references -
3 associated genes
No signs/symptoms info

COMMON GENES: 1

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

Distal hereditary motor neuropathy type 5

Autosomal dominant spastic paraplegia type 17

Citations in the biomedical literature:

Distal hereditary motor neuropathy type 5		Autosomal dominant spastic paraplegia type 17
	Synonym(s): - Distal spinal muscular atrophy type 5 - dHMN5		Synonym(s): - Distal hereditary motor neuropathy type 5B - SPG17 - Silver Syndrome - Spastic paraplegia-amyotrophy of hands and feet - dHMN5B

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

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.