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4 OMIM references -
1 associated gene
2 signs/symptoms
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Hereditary gingival fibromatosis
Phakomatosis pigmentokeratotica

SOS1 HRAS


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SOS1
(0.97)
HRAS



Citations in the biomedical literature:


Hereditary gingival fibromatosis
SOS1
Phakomatosis pigmentokeratotica
HRAS



Hereditary gingival fibromatosis
Phakomatosis pigmentokeratotica

Synonym(s):
- Autosomal dominant gingival fibromatosis
- Autosomal dominant gingival hyperplasia
- Hereditary gingival hyperplasia

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare odontologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease

Classification (ICD10):
- Diseases of the digestive system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: unknown

External references:
4 OMIM references -
No MeSH references
External references:
No OMIM references
1 MeSH reference: C537893

Hereditary gingival fibromatosis

Very frequent
- Autosomal dominant inheritance
- Thickened / hypertrophic / fibromatous gingivae



Phakomatosis pigmentokeratotica

(no data available)