Platelet Disorder, Familial, With Associated Myeloid Malignancy; Fpdmm
Genes related to Platelet Disorder, Familial, With Associated Myeloid Malignancy; Fpdmm
- RUNX1
Clinical Features
Top most frequent phenotypes and symptoms related to Platelet Disorder, Familial, With Associated Myeloid Malignancy; Fpdmm
- Anemia
- Thrombocytopenia
- Hernia
- Hypospadias
- Umbilical hernia
- Leukemia
- Bruising susceptibility
- Neutropenia
- Abnormal bleeding
- Lymphoma
And another 11 symptoms. If you need more information about this disease we can help you.
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
Platelet Disorder, Familial, With Associated Myeloid Malignancy; Fpdmm Is also known as platelet disorder, aspirin-like, thrombocytopenia, familial, with propensity to acute myelogenous leukemia, fpd/aml.
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.Platelet Disorder, Familial, With Associated Myeloid Malignancy; Fpdmm Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
RUNX1 Sequence Analysis.
By Baylor Miraca Genetics Laboratories (United States).
RUNX1
Specificity
100 %
Genes
100 % |
RUNX1 Sequence Analysis (Familial Mutation/Variant Analysis).
By Baylor Miraca Genetics Laboratories (United States).
RUNX1
Specificity
100 %
Genes
100 % |
Hereditary Leukemia/Lymphoma Panel.
By Baylor Miraca Genetics Laboratories (United States).
RUNX1, BRCA2, TP53, CBL, CEBPA, SBDS, BRIP1, PALB2, GATA2, ATM, PAX5, PRF1, PTPN11
Specificity
8 %
Genes
100 % |
Comprehensive Hereditary Cancer Panel.
By Baylor Miraca Genetics Laboratories (United States).
RUNX1, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRCA1, BRCA2, STK11, EPCAM, TP53, VHL, WT1, CBL, SUFU, CDC73, CDH1, CDK4, CDKN1C, CDKN2A , (...)
View the complete list with 39 more genes
Specificity
2 %
Genes
100 % |
Platelet Disorders.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).
RUNX1, STIM1, TBXA2R, TBXAS1, USF1, VPS33B, VWF, WAS, GP6, HPS3, HPS4, CD36, HPS5, DTNBP1, P2RY12, HPS6, MASTL, LYST, VIPAS39, FERMT3 , (...)
View the complete list with 34 more genes
Specificity
2 %
Genes
100 % |
MyeloidDx by NGS.
By Molecular Genetics Diagnostic Laboratory Detroit Medical Center University Laboratories (United States).
RUNX1, SF3B1, SRSF2, BRAF, SMC1A, STAG2, TP53, U2AF1, KDM6A, WT1, IKZF1, CALR, CBL, CBLB, SETBP1, FBXW7, CDKN2A, PHF6, ASXL1, CEBPA , (...)
View the complete list with 32 more genes
Specificity
2 %
Genes
100 % |
MyeloidDx by NGS.
By Molecular Genetics Diagnostic Laboratory Detroit Medical Center University Laboratories (United States).
RUNX1, SF3B1, SRSF2, BRAF, SMC1A, STAG2, TP53, U2AF1, KDM6A, WT1, IKZF1, CALR, CBL, CBLB, SETBP1, CBLC, FBXW7, CDKN2A, PHF6, CEBPA , (...)
View the complete list with 31 more genes
Specificity
2 %
Genes
100 % |
Inherited Bone Marrow Failure Sequencing Panel.
By Genetic Services Laboratory University of Chicago (United States).
RPL11, RPL15, RPL26, RPL35A, RPL5, RPS10, RPS19, RPS24, RPS26, RPS7, RUNX1, BRCA2, SRP72, TERC, TERT, TINF2, WAS, XRCC2, SAMD9, SAMD9L , (...)
View the complete list with 41 more genes
Specificity
2 %
Genes
100 % |
You can get up to 89 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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