ODCs

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

COMMON GENES: 1

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

Hypokalemic periodic paralysis

Thyrotoxic periodic paralysis

Citations in the biomedical literature:

Hypokalemic periodic paralysis		Thyrotoxic periodic paralysis
	Synonym(s): - Westphall disease		Synonym(s): - Thyrotoxic hypokalemic periodic paralysis

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

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

	Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: normal Type of inheritance: sporadic

	External references: 2 OMIM references - 1 MeSH reference: D020514		External references: 3 OMIM references - No MeSH references

No signs/symptoms info available.