Myeloproliferative Disorder, Chronic, With Eosinophilia

Table of contents:

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

Genes related to Myeloproliferative Disorder, Chronic, With Eosinophilia

PDGFRB

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Myeloproliferative Disorder, Chronic, With Eosinophilia

Eosinophilia
Myeloproliferative disorder
Malignant eosinophil proliferation

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

Myeloproliferative Disorder, Chronic, With Eosinophilia Is also known as mpe, emp, eosinophils, malignant proliferation of.

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.

Myeloproliferative Disorder, Chronic, With Eosinophilia Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Dystonia Exome Panel. By Genetic Services Laboratory University of Chicago (United States). BCS1L, SCN8A, SCP2, SDHA, SGCE, SLC16A2, SLC20A2, SLC2A1, SLC6A3, SLC6A8, SPR, SQSTM1, STXBP1, SUCLA2, SUOX, SURF1, SYNJ1, TAF1, TBCD, TH , (...) View the complete list with 150 more genes Panel complete gene list BCS1L, SCN8A, SCP2, SDHA, SGCE, SLC16A2, SLC20A2, SLC2A1, SLC6A3, SLC6A8, SPR, SQSTM1, STXBP1, SUCLA2, SUOX, SURF1, SYNJ1, TAF1, TBCD, TH, TIMM8A, NKX2-1, TPI1, TREX1, XK, XPR1, VPS35, FBXO7, ANO3, HTRA2, NPC2, PINK1, MICU1, DNAJC6, CBS, LRPPRC, BSCL2, KMT2B, PANK2, NDUFAF5, SAMHD1, APTX, DNAJC5, SLC19A3, PARK7, BCAP31, MCEE, COQ8A, MLC1, TPK1, ACY1, ARX, RNASEH2A, MMAA, IFIH1, VPS13A, MMAB, MECR, AARS, L2HGDH, TPP1, CLN3, CLN5, CLN6, TUBB4A, CLN8, THAP1, SLC39A14, AARS2, HACE1, SERAC1, FA2H, PDHX, COL4A1, ADAR, COX10, COX15, CP, UBA5, ADCY5, NDUFA12, RNASEH2C, TACO1, CSF1R, MMADHC, CTSD, CTSF, SLC30A10, C19orf12, VAC14, RNASEH2B, KCTD17, DCAF17, TTC19, CYP27A1, HEPACAM, FOXRED1, COX20, DDC, NDUFAF2, MFSD8, NDUFAF6, DNAJC12, WDR45, DLAT, TBC1D24, EARS2, TOR1AIP1, LIPT1, UQCRQ, COASY, ATP13A2, PRRT2, CLPB, TOR1A, AFG3L2, ECHS1, SDHAF1, FOXG1, FTL, FUCA1, GAMT, GCDH, GCH1, GLB1, GM2A, GNAL, GNAO1, GNB1, ALS2, GRN, HEXA, HIVEP2, HPCA, HPRT1, MDH2, MECP2, ARSA, MMUT, NDUFA10, NDUFA2, NDUFA9, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS7, NDUFS8, NDUFV1, NPC1, ATM, ATP1A2, ATP1A3, NUP62, PRKN, ATP7B, PDGFB, PDGFRB, PDHA1, AUH, PLA2G6, PLP1, PNKD, PNKP, POLG, PPT1, PRKRA, PSEN1, PTS, QDPR Specificity 1 % Genes 100 %
PDGFRB. Complete sequencing. By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain). PDGFRB Specificity 100 % Genes 100 %
Myeloproliferative disorder with eosinophilia (sequence analysis of PDGFRB gene). By CGC Genetics (Portugal). PDGFRB Specificity 100 % Genes 100 %
RT-PCR t(5;12) (TEL/PDGFRb). By CGC Genetics (Portugal). ETV6, PDGFRB Specificity 50 % Genes 100 %
Basal ganglia calcification, idiopathic 1 (sequence anaysis of PDGFRB gene). By CGC Genetics (Portugal). PDGFRB Specificity 100 % Genes 100 %
Detection by FISH of PDGFRB (5q32) rearrangements. By CGC Genetics (Portugal). PDGFRB Specificity 100 % Genes 100 %
Infantile myofibromatosis 1 (sequence analysis of PDGFRB gene). By CGC Genetics (Portugal). PDGFRB Specificity 100 % Genes 100 %
Idiopathic Basal Ganglia Calcification Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). SLC20A2, XPR1, PDGFB, PDGFRB Specificity 25 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

OMIM MESH Rare Disease Symptoms Checker

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