ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Spinocerebellar ataxia type 15/16

Autosomal recessive systemic lupus erythematosus

ITPR1	(UniProt - OMIM)		DNASE1L3	(UniProt - OMIM)
			PRKCD	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ITPR1	(0.56)	PRKCD

Citations in the biomedical literature:

Spinocerebellar ataxia type 15/16		Autosomal recessive systemic lupus erythematosus
	Synonym(s): - SCA15/16		Synonym(s): - Autosomal recessive SLE - Familial SLE - Familial systemic lupus erythematosus

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare systemic or rheumatologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the musculoskeletal system and connective tissue -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: no data available Type of inheritance: autosomal recessive

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

No signs/symptoms info available.