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182 Possible Causes for Familial Polycythemia

  • Myeloproliferative Disease

    Clonal hematopoiesis in familial polycythemia vera suggests the involvement of multiple mutational events in the early pathogenesis of the disease.[doi.org] […] on myeloproliferative disease with an overview of the 2016 revision of the WHO criteria for Philadelphia-chromosome negative (PCN) myeloproliferative neoplasms (MPNs) and familial[broadcastmed.com] […] polycythemiaFamilial polycythemia 30.[slideshare.net]

  • Polycythemia Vera

    ( ICD-10-CM Diagnosis Code D75.0 Familial erythrocytosis 2016 2017 2018 2019 Billable/Specific Code Applicable To Benign polycythemia Familial polycythemia Type 1 Excludes[icd10data.com] A type 1 excludes note is for used for when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition. familial polycythemia[icd10data.com] R71 Abnormality of red blood cells 2016 2017 2018 2019 Non-Billable/Non-Specific Code Type 1 Excludes anemias ( D50 - D64 ) anemia of premature infant ( P61.2 ) benign (familial[icd10data.com]

  • Familial Polycythemia

    Code Information Diagnosis Code: 289.6 Short Description: Familial polycythemia Long Description: Familial polycythemia Code Classification: Diseases of the blood and blood-forming[healthprovidersdata.com] […] myeloproliferative neoplasms in primary familial polycythemia, and secondary polycythemia (see these term).[orpha.net] […] organs (280–289) Diseases of the blood and blood-forming organs (280-289) 289 Other diseases of blood and blood-forming organs 289.6 Familial polycythemia Code Version: 2015[healthprovidersdata.com]

  • Polycythemia

    […] myeloproliferative neoplasms in primary familial polycythemia, and secondary polycythemia (see these term).[orpha.net] There are some instances in which polycythemia vera occurs in families, which results in the familial polycythemia.[seer.cancer.gov] Etiology Primary familial polycythemia is caused by mutations in the EPO receptor ( EPOR ) gene (19p13.3-p13.2) resulting in hypersensitivity to EPO.[orpha.net]

  • Secondary Polycythemia

    […] myeloproliferative neoplasms in primary familial polycythemia, and secondary polycythemia (see these term).[orpha.net] […] vera ( ICD-10-CM Diagnosis Code D45 Polycythemia vera 2016 2017 2018 2019 Billable/Specific Code Type 1 Excludes familial polycythemia ( D75.0 ) secondary polycythemia ([icd10data.com] Benign polycythemia Familial polycythemia D75.1 Secondary polycythemia Inclusion term(s): Acquired polycythemia Emotional polycythemia Erythrocytosis NOS Hypoxemic polycythemia[icd10coded.com]

  • Erythrocytosis

    polycythemia) or normal or high EPO (in secondary family polycythemias).[bloodgenetics.com] […] myeloproliferative neoplasms in primary familial polycythemia, and secondary polycythemia (see these term).[orpha.net] polycythemia congenital erythrocytosis familial polycythemia hereditary erythrocytosis primary familial polycythemia Cario H.[ghr.nlm.nih.gov]

  • Polycythemia Neonatorum

    Ophthalmia neonatorum due to gonococcus D45 Polycythemia vera excludes: familial polycythemia (D75.0) secondary polycythemia (D75.1) D75.0 Familial erythrocytosis Inclusion[codelay.com] R71 Abnormality of red blood cells 2016 2017 2018 2019 Non-Billable/Non-Specific Code Type 1 Excludes anemias ( D50 - D64 ) anemia of premature infant ( P61.2 ) benign (familial[icd10data.com] […] erythrocytosis INCLUSION TERMS: Benign polycythemia Familial polycythemia EXCLUDES1: hereditary ovalocytosis (D58.1) Familial erythrocytosis D751 Secondary polycythemia INCLUSION[gotnpi.com]

  • Stress Polycythemia

    There are some instances in which polycythemia vera occurs in families, which results in the familial polycythemia.[seer.cancer.gov] […] vera ( ICD-10-CM Diagnosis Code D45 Polycythemia vera 2016 2017 2018 2019 Billable/Specific Code Type 1 Excludes familial polycythemia ( D75.0 ) secondary polycythemia ([icd10data.com] Benign Familial Polycythemia: Rare disorder, increased erythropoietin but the bone marrow is not hyperplastic.[quizlet.com]

  • Hereditary Leiomyomatosis and Renal Cell Cancer

    An unaffected individual with a family history suggestive of HLRCC (see above) when an affected individual is unavailable for his or her own genetic testing Lab Method: Capillary[genedx.com] […] fumurate, neonatal hypotonia, growth and developmental delay, seizures, structural brain malformations, severe neurologic impairment, dysmorphic facial features, and neonatal polycythemia[genedx.com]

  • Posthemorrhagic Anaemia of the Newborn

    polycythemia Familial: benign polycythemia erythrocytosis 289.7 Methemoglobinemia Congenital NADH [DPNH]-methemoglobin-reductase deficiency Hemoglobin M [Hb-M] disease Methemoglobinemia[theodora.com] […] hemoglobin E [Hb-E] hemoglobin Zurich [Hb-Zurich] Hemoglobinopathy NOS Hereditary persistence of fetal hemoglobin [HPFH] Unstable hemoglobin hemolytic disease Excludes: familial[theodora.com] polycythemia (289.6) hemoglobin M [Hb-M] disease (289.7) high-oxygen-affinity hemoglobin (289.0) 282.8 Other specified hereditary hemolytic anemias Stomatocytosis 282.9 Hereditary[theodora.com]

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