ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Benign paroxysmal torticollis of infancy

Leukoencephalopathy - dystonia - motor neuropathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CACNA1A	(0.63)	SCP2

Citations in the biomedical literature:

Benign paroxysmal torticollis of infancy		Leukoencephalopathy - dystonia - motor neuropathy

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: normal Type of inheritance: sporadic		Epidemiological data: (no data available)

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

No signs/symptoms info available.