ODCs

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

PROTEIN INTERACTIONS: 1

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

Autosomal dominant medullary cystic kidney disease with or without hyperuricemia

Adrenocortical carcinoma

MUC1	(UniProt - OMIM)		TP53	(UniProt - OMIM)
UMOD	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MUC1	(0.7)	TP53

Citations in the biomedical literature:

Autosomal dominant medullary cystic kidney disease with or without hyperuricemia		Adrenocortical carcinoma
	Synonym(s): - Autosomal dominant nephronophthisis		Synonym(s): (no synonyms)

	Classification (Orphanet): (no data available)		Classification (Orphanet): - Rare circulatory system disease - Rare endocrine disease - Rare infertility - Rare oncologic disease - Rare renal disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: sporadic

	External references: 3 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D018268

No signs/symptoms info available.