ODCs

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1 associated gene
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

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

Benign paroxysmal torticollis of infancy

Alternating hemiplegia of childhood


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CACNA1A	(0.63)	ATP1A2

Citations in the biomedical literature:

Benign paroxysmal torticollis of infancy		Alternating hemiplegia of childhood
	Synonym(s): (no synonyms)		Synonym(s): - AHC - Alternating hemiplegia in childhood

	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: childhood Average age of death: normal Type of inheritance: sporadic		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 2 OMIM references - 1 MeSH reference: C536589

No signs/symptoms info available.