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fibromatosis, gingival, 1

Disease Summary
Associated Targets (1)
Tchem

1


GARD Rare
Mondo Description Any gingival fibromatosis in which the cause of the disease is a mutation in the SOS1 gene.
Uniprot Description A form of hereditary gingival fibromatosis, a rare condition characterized by a slow, progressive overgrowth of the gingiva. The excess gingival tissue can cover part of or the entire crown, and can result in diastemas, teeth displacement, or retention of primary or impacted teeth. GINGF1 is usually transmitted as an autosomal dominant trait, although sporadic cases are common.
Mondo Term and Equivalent IDs
MONDO:0007609:  fibromatosis, gingival, 1
GARD:0006509: 
UMLS:CN030594: