Create issue ticket

170 Possible Causes for MYH9-Related Disorder

  • Genetic Anomaly of Leukocytes

    MYH9-Related Disorders. 2008 Nov 20 [updated 2015 Jul 16].[ghr.nlm.nih.gov] GeneReview Scope MYH9 -Related Disorders: Included Phenotypes 1 Epstein syndrome Fechtner syndrome May-Hegglin anomaly Sebastian syndrome Diagnosis The MYH9 -related disorders[ncbi.nlm.nih.gov] References Althaus K, Greinacher A (2009) MYH9-related platelet disorders. SeminThrombHemost 35: 189-203.[omicsonline.org]

  • Inherited Platelet Disorder

    -Related Disorders.[ojrd.biomedcentral.com] […] protein resulting in MYH9- related disorder (Epstein syndrome).[intechopen.com] MYH9-related platelet disorders. Semin Thromb Hemost. 2009;35(2):189–203. PubMed PMID: 19408192. CrossRef PubMed Google Scholar Balduini CL, Pecci A, Noris P.[link.springer.com]

  • Congenital Deafness

    ., Cheong, H.I. (2011) Renal manifestations of patients with MYH9-related disorders.[scindeks.ceon.rs] -related disorders.[scindeks.ceon.rs] Pediatr Blood Cancer, 58(2): 314-5 [ CR ] [ PM ] [ EČ ][ GS ] Singh, N., Nainani, N., Arora, P., Venuto, R.C. (2009) CKD in MYH9-related disorders.[scindeks.ceon.rs]

  • 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]

  • Winchester Syndrome

    -related disorder MYH9-related macrothrombocytopenias , see MYH9-related disorder MYH9RD , see MYH9-related disorder Myhre syndrome Myhre-Riley-Smith syndrome , see Bannayan-Riley-Ruvalcaba[herenciageneticayenfermedad.blogspot.com] […] acute promyelocytic leukemia myeloid metaplasia , see primary myelofibrosis myelomatosis , see multiple myeloma MYH-associated polyposis , see familial adenomatous polyposis MYH9[herenciageneticayenfermedad.blogspot.com]

  • Benign Adult Familial Myoclonic Epilepsy

    RD MYH9-related disease MYH9-related disorder MYH9-related syndrome MYH9-related syndromic thrombocytopenia Myhre-Riley-Smith syndrome Myhre syndrome Myiasis MYO5B deficiency[orpha.net] Myeloproliferative neoplasm MYH7-related late-onset scapuloperoneal muscular dystrophy MYH7-related late-onset scapuloperoneal syndrome MYH7-related late-onset SPMD MYH9-[orpha.net] […] neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB or FGFR1 Myeloid sarcoma Myelomatosis Myelomeningocele Myeloperoxidase deficiency Myeloproliferative disorder[orpha.net]

  • Unverricht-Lundborg Syndrome

    RD MYH9-related disease MYH9-related disorder MYH9-related syndrome MYH9-related syndromic thrombocytopenia Myhre-Riley-Smith syndrome Myhre syndrome Myiasis MYO5B deficiency[orpha.net] Myeloproliferative neoplasm MYH7-related late-onset scapuloperoneal muscular dystrophy MYH7-related late-onset scapuloperoneal syndrome MYH7-related late-onset SPMD MYH9-[orpha.net] […] neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB or FGFR1 Myeloid sarcoma Myelomatosis Myelomeningocele Myeloperoxidase deficiency Myeloproliferative disorder[orpha.net]

  • Hereditary Neutrophilia

    NIH: National Library of Medicine Genetics (Medical Encyclopedia) [ Read More ] MYH9-related disorder MYH9-related disorder is a condition that can have many signs and symptoms[icdlist.com] All individuals with MYH9-related disorder have thrombocytopenia and enlarged platelets.[icdlist.com] The first sign of renal disease in MYH9-related disorder is typically protein or blood in the urine.[icdlist.com]

  • HIV-induced Thrombocytopenia

    MYH9-related disorders. Myosin heavy chain 9 (MYH9)-related platelet diseases belong to the group of inherited thrombocytopenia.[thrombocyte.com]

  • Platelet-Type Bleeding Disorder 19

    MYH9-related platelet disorders. Semin Thromb Hemost. 2009; 35 (2): 189-203[ DOI ][ PubMed ] 7. Balduini CL, Pecci A, Savoia A.[ijp.tums.pub] 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] Additional thrombocytopenia-related conditions are caused by mutations in MYH9, encoding nonmuscular myosin heavy chain 9 protein: Epstein syndrome is an autosomal dominant[centogene.com]

Further symptoms