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Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
3 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Pilomatrixoma
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Pilomatrixoma

MUC1
(UniProt - OMIM)
 CTNNB1
(UniProt - OMIM)
UMOD
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MUC1
(0.9)
CTNNB1


Citations in the biomedical literature:


Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
MUC1 UMOD
Pilomatrixoma
CTNNB1



Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Pilomatrixoma

Synonym(s):
- Autosomal dominant nephronophthisis
Synonym(s):
- Epithelioma calcificans of Malherbe
- Pilomatricoma
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare oncologic disease
- Rare skin disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -
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:
(no data available)
External references:
3 OMIM references -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D018296
No signs/symptoms info available.