Fibromatosis, Gingival, 5; Gingf5

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Description

Gingival fibromatosis-5 is an autosomal dominant benign overgrowth disorder characterized by slowly progressive fibrous enlargement of the keratinized gingival tissues. Affected individuals may have diastema, malposition of the teeth, and prolonged retention of primary teeth. Onset is in the first decade. Treatment by surgical resection is generally followed by regrowth of the gingival tissues (summary by Pehlivan et al., 2009).

Genes related to Fibromatosis, Gingival, 5; Gingf5

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Clinical Features

Top most frequent phenotypes and symptoms related to Fibromatosis, Gingival, 5; Gingf5

Short stature
Hernia
Osteoporosis
Respiratory tract infection
Overgrowth
Gingival overgrowth
Recurrent upper respiratory tract infections
Osteomyelitis
Abnormality of the sternum
Hiatus hernia

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Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Alternative names

Fibromatosis, Gingival, 5; Gingf5 Is also known as ggf5, hgf5, fibromatosis, gingival, hereditary, 5.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Fibromatosis, Gingival, 5; Gingf5 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Cancer Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). RUNX1, BLM, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRCA1, BRCA2, SMARCA4, SMARCB1, SMARCE1, SRP72, STK11, EPCAM, TERC, TERT, TP53, TRIP13, TSC1 , (...) View the complete list with 78 more genes Panel complete gene list RUNX1, BLM, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRCA1, BRCA2, SMARCA4, SMARCB1, SMARCE1, SRP72, STK11, EPCAM, TERC, TERT, TP53, TRIP13, TSC1, TSC2, VHL, WT1, XRCC2, SAMD9L, SUFU, KIF1B, CDC73, PALLD, DICER1, POT1, CDH1, CDK4, CDKN1B, CDKN1C, CDKN2A, CEBPA, DDX41, GALNT12, GREM1, BRIP1, ARMC5, SDHAF2, TMEM127, PALB2, FLCN, DIS3L2, ANKRD26, ETV6, EXT1, EXT2, AIP, FANCC, FH, GATA2, ALK, GPC3, HOXB13, HRAS, APC, KIT, LZTR1, SMAD4, MAX, MEN1, MET, MITF, MLH1, MLH3, MRE11, MSH2, MSH3, MSH6, MUTYH, NBN, NF1, NF2, ATM, NTHL1, PDGFRA, AXIN2, PMS2, PHOX2B, POLD1, POLE, PRKAR1A, BAP1, BARD1, PTCH1, PTCH2, PTEN, RAD50, RAD51C, RAD51D, RB1, RECQL, REST, RET Specificity 2 % Genes 100 %
REST. By Fulgent Genetics Fulgent Genetics (United States). REST Specificity 100 % Genes 100 %
Hereditary Pediatric Cancer Panel. By Blueprint Genetics (Finland). RIT1, RRAS, RUNX1, BLM, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRAF, SMARCA4, SMARCB1, SOS1, SOS2, STK11, BUB1B, EPCAM, TP53, TSC1, TSC2 , (...) View the complete list with 51 more genes Panel complete gene list RIT1, RRAS, RUNX1, BLM, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRAF, SMARCA4, SMARCB1, SOS1, SOS2, STK11, BUB1B, EPCAM, TP53, TSC1, TSC2, VHL, WRN, WT1, NSD1, CBL, SHOC2, SUFU, CDC73, DICER1, CDKN1C, CEBPA, NSUN2, SDHAF2, TMEM127, DIS3L2, EZH2, FH, GATA2, ALK, GPC3, HRAS, APC, KRAS, LZTR1, SMAD4, MAP2K1, MAP2K2, MAX, MEN1, MLH1, MSH2, MSH6, NBN, NF1, NF2, NRAS, PAX5, AXIN2, PMS2, PHOX2B, PRF1, PRKAR1A, BAP1, PTCH1, PTEN, PTPN11, RAF1, RASA2, RECQL4, REST, RET Specificity 2 % Genes 100 %
Comprehensive Hereditary Cancer Panel. By Blueprint Genetics (Finland). RIT1, RRAS, RUNX1, BLM, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRAF, BRCA1, BRCA2, SMARCA4, SMARCB1, SOS1, SOS2, SRP72, STK11, BUB1B, EPCAM , (...) View the complete list with 125 more genes Panel complete gene list RIT1, RRAS, RUNX1, BLM, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRAF, BRCA1, BRCA2, SMARCA4, SMARCB1, SOS1, SOS2, SRP72, STK11, BUB1B, EPCAM, HNF1A, TERC, TERT, TINF2, CD70, TP53, TSC1, TSC2, VHL, WRN, WT1, XPA, XPC, XRCC2, IKZF1, SAMD9L, NSD1, CBL, SHOC2, SUFU, CDC73, DICER1, POT1, CDH1, CDK4, CDKN1B, CDKN1C, CDKN2A, CEBPA, DDX41, SBDS, GREM1, SPRED1, BRIP1, FANCL, RHBDF2, FANCM, SLX4, FANCI, CYLD, NSUN2, SDHAF2, TMEM127, PALB2, DDB2, FLCN, DIS3L2, DKC1, ANKRD26, CEP57, EGFR, ELANE, ERCC1, ERCC2, ERCC3, ERCC4, ERCC5, ETV6, EXO1, EXT1, EXT2, EZH2, AIP, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FH, GATA2, ALK, GPC3, HOXB13, HRAS, APC, KIT, KITLG, KRAS, LZTR1, SMAD4, MAP2K1, MAP2K2, MAX, MEN1, MET, MITF, MLH1, MLH3, MRE11, MSH2, MSH6, MUTYH, NBN, NF1, NF2, ATM, NRAS, NTHL1, PAX5, PDGFRA, AXIN2, PMS1, PMS2, PHOX2B, POLD1, POLE, POLH, PPM1D, PRF1, PRKAR1A, BAP1, BARD1, PTCH1, PTEN, PTPN11, RAD50, RAD51C, RAD51D, RAF1, RASA2, RECQL4, REST, RET Specificity 1 % Genes 100 %
Hereditary Renal Cancer Panel. By Blueprint Genetics (Finland). SDHB, SDHC, SDHD, SMARCA4, SMARCB1, EPCAM, TP53, TSC1, TSC2, VHL, WT1, CDC73, DICER1, CDKN1C, FLCN, DIS3L2, FH, GPC3, MET, MLH1 , (...) View the complete list with 6 more genes Panel complete gene list SDHB, SDHC, SDHD, SMARCA4, SMARCB1, EPCAM, TP53, TSC1, TSC2, VHL, WT1, CDC73, DICER1, CDKN1C, FLCN, DIS3L2, FH, GPC3, MET, MLH1, MSH2, MSH6, PMS2, BAP1, PTEN, REST Specificity 4 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

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