ODCs

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

PROTEIN INTERACTIONS: 1

6 associated genes
No signs/symptoms info

Autosomal recessive spastic paraplegia type 18

Familial renal cell carcinoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ERLIN2	(0.63)	RNF139

Citations in the biomedical literature:

Autosomal recessive spastic paraplegia type 18		Familial renal cell carcinoma
	Synonym(s): - SPG18		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): (no data available)

	Classification (ICD10): - Diseases of the nervous system -		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: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references 1 MeSH reference: C536851

No signs/symptoms info available.