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225 Possible Causes for MYH9-Related Disease

  • Genetic Anomaly of Leukocytes

    related disease.[journals.plos.org] Brief Summary: The term MYH9-related disease (MYH9RD) includes four genetic disorders: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome.[clinicaltrials.gov] -related disease.[omicsonline.org]

  • Thrombocytopenia

    Abstract MYH9-related disease (MYH9-RD) is an inherited rare autosomal dominant macrothrombocytopenia.[ncbi.nlm.nih.gov] D69.4 MYH9-related disease D69.42 Congenital thrombotic thrombocytopenic purpura D82.0 Wiskott-Aldrich syndrome D69.4 Familial platelet syndrome with predisposition to acute[blueprintgenetics.com] Grey platelet syndrome Macrothrombocytopenia and hearing loss May-Hegglin anomaly MYH9-related disease PRKACG-related thrombocytopenia Paris-Trousseau thrombocytopenia/Jacobsen[en.wikipedia.org]

  • Platelet-Type Bleeding Disorder 19

    ABSTRACT MYH9 -related disease is an autosomal dominant disorder caused by mutations of the MYH9 gene, which encodes the non-muscle myosin heavy chain IIA on chromosome 22q12[ncbi.nlm.nih.gov] Abstract MYH9 related diseases are caused by mutations in the MYH9 gene and constitute a rare group of genetic entities.[revistanefrologia.com] The first type is characterized by syndromic features associated with mutations in genes encoding myosin IIA in myosin heavy chain 9 (MYH9)-related disease, filamin-A (FLNa[doi.org]

  • Congenital Deafness

    -related disorders.[scindeks.ceon.rs] (HDR) Sensorineural deafness CaSR Hypo-/hyper-parathyroidism a Epstein and Fechtner syndromes are considered variable expressions of a single illness: ‘ MYH9 -related disease[academic.oup.com] ., Cheong, H.I. (2011) Renal manifestations of patients with MYH9-related disorders.[scindeks.ceon.rs]

  • Inherited Platelet Disorder

    -Related Disorders.[ojrd.biomedcentral.com] -related disease (MYH9-RD) patients. 26 – 28 The aim of the Surgery in Platelet disorders And Therapeutic Approach (SPATA) study was to evaluate the bleeding complications[haematologica.org] Genetic confirmation of MYH9 -related disorders, therefore, has prognostic significance.[intechopen.com]

  • May-Thurner Syndrome

    , May-Hegglin異常 【類義語】 Epstein syndrome , Fechtner syndrome , MYH9-related disease, MYH9-related disorder , Sebastian syndrome May-Thurner syndrome シソーラス PubMed , Scholar ,[lsd-project.jp] […] may ***** コーパス (助動詞;過去might)(可能性)… だろう , (推量)… かも知れない 【類義語】 might , shall , will May-Hegglin anomaly * シソーラス PubMed , Scholar , Google , WikiPedia (MYH9関連疾患の別名) メイ・ヘグリン異常[lsd-project.jp]

  • Psychomotor Retardation

    MYH9-related disease.[sjkdt.org]

  • Unverricht-Lundborg Syndrome

    […] late-onset scapuloperoneal muscular dystrophy MYH7-related late-onset scapuloperoneal syndrome MYH7-related late-onset SPMD MYH9-RD MYH9-related disease MYH9-related disorder[orpha.net] […] abnormality of PDGFRA, PDGFRB or FGFR1 Myeloid sarcoma Myelomatosis Myelomeningocele Myeloperoxidase deficiency Myeloproliferative disorder Myeloproliferative neoplasm MYH7-related[orpha.net]

  • Benign Adult Familial Myoclonic Epilepsy

    […] late-onset scapuloperoneal muscular dystrophy MYH7-related late-onset scapuloperoneal syndrome MYH7-related late-onset SPMD MYH9-RD MYH9-related disease MYH9-related disorder[orpha.net] […] abnormality of PDGFRA, PDGFRB or FGFR1 Myeloid sarcoma Myelomatosis Myelomeningocele Myeloperoxidase deficiency Myeloproliferative disorder Myeloproliferative neoplasm MYH7-related[orpha.net]

  • Familial Interstitial Nephritis

    MYH9-related disease.[sjkdt.org]

Further symptoms