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Oligodontia - cancer predisposition syndrome
1 OMIM reference -
1 associated gene
11 connected diseases
No signs/symptoms info
Disease Type of connection
Oligodontia
Desmoid tumor
APC-related attenuated familial adenomatous polyposis
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Familial adenomatous polyposis due to 5q22.2 microdeletion
Gardner syndrome
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Turcot syndrome with polyposis
Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis
Synonym(s):
- Autosomal dominant ectodermal dysplasia-cancer predisposition syndrome syndrome
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare odontologic disease
- Rare oncologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
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
AXIN2 Q9Y2T1604025
No signs/symptoms info available.