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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
Craniopharyngioma
2 associated genes
No signs/symptoms info
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Craniopharyngioma

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



Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Craniopharyngioma

Synonym(s):
- Autosomal dominant nephronophthisis
Synonym(s):
(no synonyms)
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare endocrine disease
- Rare neurologic disease
- Rare oncologic 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:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic
External references:
3 OMIM references -
No MeSH references
External references:
No OMIM references
1 MeSH reference: D003397
No signs/symptoms info available.