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MUTYH-related attenuated familial adenomatous polyposis
1 OMIM reference -
1 associated gene
7 connected diseases
No signs/symptoms info
Disease Type of connection
Familial gastric cancer
Constitutional mismatch repair deficiency syndrome
Hereditary nonpolyposis colon cancer
Muir-Torre syndrome
Non-polyposis Turcot syndrome
Autosomal dominant Charcot-Marie-Tooth disease type 2P
Intellectual deficit, X-linked, Turner type
Synonym(s):
- MUTYH-related AFAP
- MUTYH-related attenuated FAP
- MUTYH-related attenuated familial polyposis coli
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
MUTYH Q9UIF7604933
No signs/symptoms info available.