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

APC
(UniProt - OMIM)
 MUC1
(UniProt - OMIM)
UMOD
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
APC
(0.73)
MUC1


Citations in the biomedical literature:


Gardner syndrome
APC
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
MUC1 UMOD



Gardner syndrome
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia

Synonym(s):
(no synonyms)

Synonym(s):
- Autosomal dominant nephronophthisis
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
(no data available)
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: D005736
External references:
3 OMIM references -
No MeSH references
No signs/symptoms info available.