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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
6 OMIM references -
10 associated genes
8 signs/symptoms
Gardner syndrome
Oligodontia

APC AXIN2
EDA
EDARADD
FGFR1
IRF6
LTBP3
MSX1
PAX9
TGFA
WNT10A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APC
(0.63)
AXIN2



Citations in the biomedical literature:


Gardner syndrome
APC
Oligodontia
AXIN2 EDA EDARADD FGFR1 IRF6 LTBP3
MSX1 PAX9 TGFA WNT10A



Gardner syndrome
Oligodontia

Synonym(s):
(no synonyms)

Synonym(s):
- Selective tooth agenesis

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 genetic disease
- Rare odontologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the digestive system -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: D005736
External references:
6 OMIM references -
No MeSH references

Oligodontia

Very frequent
- Anodontia / oligodontia / hypodontia
- Complete / partial microdontia
- Face / facial anomalies
- Hypoplastic mandibula / partial absence of the mandibula
- Tooth shape anomaly

Frequent
- Autosomal dominant inheritance
- Autosomal recessive inheritance
- X-linked recessive inheritance



Gardner syndrome

(no data available)