ODCs

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

PROTEIN INTERACTIONS: 1

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

Autosomal dominant spastic paraplegia type 10

Hypokalemic periodic paralysis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KIF5A	(0.63)	KCNE3

Citations in the biomedical literature:

Autosomal dominant spastic paraplegia type 10		Hypokalemic periodic paralysis
	Synonym(s): - SPG10		Synonym(s): - Westphall 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: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: C537482		External references: 2 OMIM references - 1 MeSH reference: D020514

No signs/symptoms info available.