ODCs

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

PROTEIN INTERACTIONS: 1

2 associated genes
No signs/symptoms info

Inherited congenital spastic tetraplegia

Craniopharyngioma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KANK1	(0.63)	CTNNB1

Citations in the biomedical literature:

Inherited congenital spastic tetraplegia		Craniopharyngioma
	Synonym(s): - Inherited congenital spastic quadriplegia		Synonym(s): (no synonyms)

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

	Classification (ICD10): (no data available)		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: variable Average age of death: - Type of inheritance: sporadic

	External references: 2 OMIM references - No MeSH references		External references: No OMIM references 1 MeSH reference: D003397

No signs/symptoms info available.