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Gardner syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Inflammatory myofibroblastic tumor
6 associated genes
No signs/symptoms info
Gardner syndrome
Inflammatory myofibroblastic tumor

APC
(UniProt - OMIM)
 ALK
(UniProt - OMIM)
CARS
(UniProt - OMIM)
CLTC
(UniProt - OMIM)
RANBP2
(UniProt - OMIM)
TPM3
(UniProt - OMIM)
TPM4
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
APC
(0.82)
RANBP2


Citations in the biomedical literature:


Gardner syndrome
APC
Inflammatory myofibroblastic tumor
ALK CARS CLTC RANBP2 TPM3 TPM4



Gardner syndrome
Inflammatory myofibroblastic tumor

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: D005736
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.