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GTR Home > Conditions/Phenotypes > Fibromatosis, gingival, 1

Fibromatosis, gingival, 1

Synonyms: Hereditary gingival fibromatosis, 1

Summary

Any gingival fibromatosis in which the cause of the disease is a mutation in the SOS1 gene. [from MONDO]

Available tests

45 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (45 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

SOS1
206 tests
Also known as: GF1, GGF1, GINGF, HGF, NS4, SOS-1, SOS1
Summary: SOS Ras/Rac guanine nucleotide exchange factor 1

Imported from Human Phenotype Ontology (HPO)

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Abnormality of the nervous system
- Intellectual disability
  Intellectual disability
  - MedGen UID: 811461
  - Concept ID: C3714756
  - Finding: Mental or Behavioral Dysfunction
  Abnormality of the nervous system
  See: Feature record | Search on this feature
Ear malformation
- Hearing impairment
  Hearing impairment
  - MedGen UID: 235586
  - Concept ID: C1384666
  - Finding: Disease or Syndrome
  Ear malformation
  See: Feature record | Search on this feature
Neoplasm
- Gingival fibromatosis
  Gingival fibromatosis
  - MedGen UID: 42017
  - Concept ID: C0016049
  - Finding: Finding
  Neoplasm
  See: Feature record | Search on this feature

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