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141 Possible Causes for RASA2

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  • Noonan Syndrome 1

    These genes are included in CENTOGENE s Noonan - CFC syndrome panel (BRAF, CBL, HRAS, KAT6B, KRAS, LZTR1, MAP2K1, MAP2K2, NF1, NRAS, PTPN11, RAF1, RASA2, RIT1, SHOC2, SOS1[centogene.com] […] panel that includes assessment of selected non-coding disease-causing variants This Panel covers many recently discovered rasopathy genes such as RRAS, PPP1CB, NRAS , and RASA2[blueprintgenetics.com] […] type IV AD 4 PTPN11 176876 LEOPARD syndrome 1; Noonan syndrome 1; Leukemia, juvenile myelomonocytic AD 12 RAF1 164760 Noonan syndrome 5; Cardiomyopathy, dilated, 1NN AD 8 RASA2[centogene.com]

  • Young Simpson Syndrome

    Forms and Documents Test Details Genes: A2ML1, ACTB, ACTG1, BRAF, CBL, HRAS, KAT6B, KRAS, LZTR1, MAP2K1, MAP2K2, NF1, NRAS, NSUN2, PPP1CB, PTPN11, RAF1, RASA1, RASA2, RIT1[genedx.com] 3611-msv v-raf-1 murine leukemia viral oncogene homolog 1 RAF1 C-RAF CRAF RAF-1 164760 9829 RAS p21 protein activator 1 RASA1 RASA 139150 9871 RAS p21 protein activator 2 RASA2[ukgtn.nhs.uk]

  • Baraitser Syndrome

    Forms and Documents Test Details Genes: A2ML1, ACTB, ACTG1, BRAF, CBL, HRAS, KAT6B, KRAS, LZTR1, MAP2K1, MAP2K2, NF1, NRAS, NSUN2, PPP1CB, PTPN11, RAF1, RASA1, RASA2, RIT1[genedx.com]

  • Amelogenesis Imperfecta Type 1G with Nephrocalcinosis

    COL9A2, COL11A1, COL11A2, POLR1C, TCOF1, CHSY1, POLR1D, LZTR1, PEX14, PEX19, KAT6B, WDR35, CANT1, PTH1R, MBTPS2, FANCB, EBP, SOX3, NSDHL, POR, MSX2, TWIST1, COMP, SOX9, RASA2[mendelian.co]

  • Neurofibromatosis-Noonan Syndrome

    These genes are included in CENTOGENE s Noonan - CFC syndrome panel (BRAF, CBL, HRAS, KAT6B, KRAS, LZTR1, MAP2K1, MAP2K2, NF1, NRAS, PTPN11, RAF1, RASA2, RIT1, SHOC2, SOS1[centogene.com] […] panel that includes assessment of selected non-coding disease-causing variants This Panel covers many recently discovered rasopathy genes such as RRAS, PPP1CB, NRAS , and RASA2[blueprintgenetics.com] 3611-msv v-raf-1 murine leukemia viral oncogene homolog 1 RAF1 C-RAF CRAF RAF-1 164760 9829 RAS p21 protein activator 1 RASA1 RASA 139150 9871 RAS p21 protein activator 2 RASA2[ukgtn.nhs.uk]

  • Spondyloepimetaphyseal Dysplasia Type Geneviève

    COL9A2, COL11A1, COL11A2, POLR1C, TCOF1, CHSY1, POLR1D, LZTR1, PEX14, PEX19, KAT6B, WDR35, CANT1, PTH1R, MBTPS2, FANCB, EBP, SOX3, NSDHL, POR, MSX2, TWIST1, COMP, SOX9, RASA2[mendelian.co]

  • 10q22.3q23.3 Microduplication Syndrome

    These genes are included in CENTOGENE s Noonan - CFC syndrome panel (BRAF, CBL, HRAS, KAT6B, KRAS, LZTR1, MAP2K1, MAP2K2, NF1, NRAS, PTPN11, RAF1, RASA2, RIT1, SHOC2, SOS1[centogene.com] […] type IV AD 4 PTPN11 176876 LEOPARD syndrome 1; Noonan syndrome 1; Leukemia, juvenile myelomonocytic AD 12 RAF1 164760 Noonan syndrome 5; Cardiomyopathy, dilated, 1NN AD 8 RASA2[centogene.com] SPRED1 609291 Legius syndrome AD 16 CENTOGENE offers the Noonan - CFC syndrome panel (genes: BRAF, CBL, HRAS, KAT6B, KRAS, LZTR1, MAP2K1, MAP2K2, NF1, NRAS, PTPN11, RAF1, RASA2[centogene.com]

  • Familial Thoracic Aortic Aneurysm 1

    Noonan syndrome with multiple lentigines MONDO:0007893 SOP5 No Reported Evidence 06/07/2018 RASA2 Costello syndrome MONDO:0009026 SOP5 No Reported Evidence 06/07/2018 RASA2[clinicalgenome.org] […] cardiofaciocutaneous syndrome MONDO:0015280 SOP5 No Reported Evidence 06/07/2018 RASA2 Noonan syndrome MONDO:0018997 SOP5 Limited 07/24/2018 RASA2 Noonan syndrome-like disorder[clinicalgenome.org] […] syndrome MONDO:0009026 SOP5 No Reported Evidence 06/07/2018 RASA1 Noonan syndrome-like disorder with loose anagen hair MONDO:0011899 SOP5 No Reported Evidence 06/07/2018 RASA2[clinicalgenome.org]

  • Loeys-Dietz Syndrome Type 2

    Noonan syndrome with multiple lentigines MONDO:0007893 SOP5 No Reported Evidence 06/07/2018 RASA2 Costello syndrome MONDO:0009026 SOP5 No Reported Evidence 06/07/2018 RASA2[clinicalgenome.org] […] cardiofaciocutaneous syndrome MONDO:0015280 SOP5 No Reported Evidence 06/07/2018 RASA2 Noonan syndrome MONDO:0018997 SOP5 Limited 07/24/2018 RASA2 Noonan syndrome-like disorder[clinicalgenome.org] […] syndrome MONDO:0009026 SOP5 No Reported Evidence 06/07/2018 RASA1 Noonan syndrome-like disorder with loose anagen hair MONDO:0011899 SOP5 No Reported Evidence 06/07/2018 RASA2[clinicalgenome.org]

  • Adams-Oliver Syndrome 5

    RAB40AL, ZDHHC9, BRWD3, CLIC2, SLC16A2, SOX3, NAA10, NSDHL, ARHGEF6, ZNF81, IL1RAPL1, KLF8, LAS1L, EIF2S3, ZMYM3, CLCN4, CCDC22, THOC2, RAB23, POR, TWIST1, SPRED1, NSUN2, RASA2[mendelian.co] COL9A2, COL11A1, COL11A2, POLR1C, TCOF1, CHSY1, POLR1D, LZTR1, PEX14, PEX19, KAT6B, WDR35, CANT1, PTH1R, MBTPS2, FANCB, EBP, SOX3, NSDHL, POR, MSX2, TWIST1, COMP, SOX9, RASA2[mendelian.co]

Further symptoms