ODCs

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4 OMIM references -
1 associated gene
2 signs/symptoms

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Hereditary gingival fibromatosis

Combined immunodeficiency due to ZAP70 deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SOS1	(0.55)	ZAP70

Citations in the biomedical literature:

Hereditary gingival fibromatosis		Combined immunodeficiency due to ZAP70 deficiency
	Synonym(s): - Autosomal dominant gingival fibromatosis - Autosomal dominant gingival hyperplasia - Hereditary gingival hyperplasia		Synonym(s): - Zeta-associated-protein 70 deficiency

	Classification (Orphanet): - Rare genetic disease - Rare odontologic disease		Classification (Orphanet): - Rare genetic disease - Rare immune disease

	Classification (ICD10): - Diseases of the digestive system -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	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: childhood Average age of death: - Type of inheritance: autosomal recessive

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

Hereditary gingival fibromatosis
	Very frequent - Autosomal dominant inheritance - Thickened / hypertrophic / fibromatous gingivae
Combined immunodeficiency due to ZAP70 deficiency
(no data available)