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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Gardner syndrome
Commissural facial cleft

APC PTCH2
SPECC1L


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APC
(0.63)
SPECC1L



Citations in the biomedical literature:


Gardner syndrome
APC
Commissural facial cleft
PTCH2 SPECC1L



Gardner syndrome
Commissural facial cleft

Synonym(s):
(no synonyms)

Synonym(s):
- Macrostomia

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 developmental defect during embryogenesis
- Rare genetic disease
- Rare maxillo-facial surgical disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

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

No signs/symptoms info available.