ODCs

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

COMMON GENES: 1

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

Autosomal dominant spastic paraplegia type 31

Distal hereditary motor neuropathy type 5

Citations in the biomedical literature:

Autosomal dominant spastic paraplegia type 31		Distal hereditary motor neuropathy type 5
	Synonym(s): - SPG31		Synonym(s): - Distal spinal muscular atrophy type 5 - dHMN5

	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: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.