Plasma Fibronectin Deficiency
Clinical Features
Phenotypes and symptoms related to Plasma Fibronectin Deficiency
- Abnormal bleeding
- Keloids
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.
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.Plasma Fibronectin Deficiency Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
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Glomerulopathy with Fibronectin Deposits via FN1 Gene Sequencing with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
FN1
Specificity
100 %
Genes
100 % |
Spondylo-Epi-Metaphyseal dysplasias Deletion / Duplication panel.
By Connective Tissue Gene Tests (United States).
RMRP, BGN, RUNX2, SLC26A2, SMARCAL1, ACP5, CFAP410, CCN6, XYLT1, RAB33B, B3GALT6, TRPV4, NANS, SBDS, CHST3, CANT1, DYM, COL10A1, COL11A1, COL11A2 , (...)
View the complete list with 33 more genes
Specificity
2 %
Genes
100 % |
Spondylo-Epi-Metaphyseal dysplasias Comprehensive panel.
By Connective Tissue Gene Tests (United States).
RMRP, BGN, RUNX2, SLC26A2, SMARCAL1, ACP5, CFAP410, CCN6, XYLT1, RAB33B, B3GALT6, TRPV4, NANS, SBDS, CHST3, CANT1, DYM, COL10A1, COL11A1, COL11A2 , (...)
View the complete list with 33 more genes
Specificity
2 %
Genes
100 % |
Spondylo-Epi-Metaphyseal dysplasias NGS panel.
By Connective Tissue Gene Tests (United States).
RMRP, BGN, RUNX2, SLC26A2, SMARCAL1, ACP5, CFAP410, CCN6, XYLT1, RAB33B, B3GALT6, TRPV4, NANS, SBDS, CHST3, CANT1, DYM, COL10A1, COL11A1, COL11A2 , (...)
View the complete list with 33 more genes
Specificity
2 %
Genes
100 % |
Nephrotic syndrome and related disorders Comprehensive panel.
By Connective Tissue Gene Tests (United States).
SGPL1, SMARCAL1, TRPC6, WT1, NPHS2, ANLN, CD2AP, ACTN4, SCARB2, PLCE1, NUP205, CRB2, MAGI2, COQ8B, COQ6, COL4A3, COL4A4, COL4A5, COL4A6, PDSS2 , (...)
View the complete list with 22 more genes
Specificity
3 %
Genes
100 % |
Nephrotic syndrome and related disorders NGS panel.
By Connective Tissue Gene Tests (United States).
SGPL1, SMARCAL1, TRPC6, WT1, NPHS2, ANLN, CD2AP, ACTN4, SCARB2, PLCE1, NUP205, CRB2, MAGI2, COQ8B, COQ6, COL4A3, COL4A4, COL4A5, COL4A6, PDSS2 , (...)
View the complete list with 22 more genes
Specificity
3 %
Genes
100 % |
Nephrotic syndrome and related disorders Deletion / Duplication panel.
By Connective Tissue Gene Tests (United States).
SGPL1, SMARCAL1, TRPC6, WT1, NPHS2, ANLN, CD2AP, ACTN4, SCARB2, PLCE1, NUP205, CRB2, MAGI2, COQ8B, COQ6, COL4A3, COL4A4, COL4A5, COL4A6, PDSS2 , (...)
View the complete list with 22 more genes
Specificity
3 %
Genes
100 % |
Hereditary kidney disorders - different panels.
By Institute of Human Genetics Uniklinik RWTH Aachen (Germany).
BCS1L, ROBO2, CNNM2, CFB, SALL1, ATXN10, SCNN1A, SCNN1B, SCNN1G, SDCCAG8, SDHA, SDHB, SDHC, SDHD, BMP4, BMP7, SGPL1, SIX1, SIX2, SIX5 , (...)
View the complete list with 386 more genes
Specificity
1 %
Genes
100 % |
You can get up to 4 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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