"haemoglobinopathy" meaning in All languages combined

See haemoglobinopathy on Wiktionary

Noun [English]

IPA: /ˌhiːməˌɡləʊbɪˈnɒpəθi/ [Received-Pronunciation], /ˌhiməˌɡloʊbɪˈnɑpəθi/ [General-American] Forms: haemoglobinopathies [plural]
Rhymes: -ɒpəθi Etymology: From haemoglobin + -o- + -pathy. Etymology templates: {{af|en|haemoglobin|-o-|-pathy}} haemoglobin + -o- + -pathy Head templates: {{en-noun|~}} haemoglobinopathy (countable and uncountable, plural haemoglobinopathies)
  1. (British spelling, medicine) Any of a group of inherited disorders in which haemoglobin does not function properly Wikipedia link: Hemoglobinopathy Tags: UK, countable, uncountable Categories (topical): Medicine Synonyms: hemoglobinopathy

Inflected forms

Download JSON data for haemoglobinopathy meaning in All languages combined (3.2kB)

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      "name": "af"
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  ],
  "etymology_text": "From haemoglobin + -o- + -pathy.",
  "forms": [
    {
      "form": "haemoglobinopathies",
      "tags": [
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  "head_templates": [
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      "args": {
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  "lang_code": "en",
  "pos": "noun",
  "senses": [
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        {
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          "name": "English entries with incorrect language header",
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      "examples": [
        {
          "ref": "1996 December 7, Geoffrey Pasvol, “Malaria and resistance genes—they work in wondrous ways”, in The Lancet, volume 348, number 9041, →DOI, page 1533",
          "text": "Simpler tools for detecting sickle haemoglobin made analysis of the malaria hypothesis in the context of this haemoglobinopathy that much easier, which has facilitated measurement of the trait against a spectrum of endpoints of protection, such as the infection itself, parasite density in infection, uncomplicated disease, and severe disease, and death.",
          "type": "quotation"
        },
        {
          "ref": "2000 February 29, Joseph Telfair, Marilyn Gardner, “Adolescents with Sickle Cell Disease: Determinants of Support Group Attendance and Satisfaction”, in Health & Social Work, →DOI, page 44",
          "text": "Active group membership was operationalized as having attended at least one group meeting during the past year, requesting voluntary inclusion on the group’s roster, and having been formally diagnosed with SCD or a related hemoglobinopathy.",
          "type": "quotation"
        },
        {
          "ref": "2016 December 19, Emmanuel Bissé et al., “Hemoglobin Kirklareli (α H58L), a New Variant Associated with Iron Deficiency and Increased CO Binding”, in Journal of Biological Chemistry, →DOI, page 2548",
          "text": "The clinical phenotypes of over 125 different hemoglobinopathies were interpreted in terms of structural alterations in globin structure.",
          "type": "quotation"
        }
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        "Any of a group of inherited disorders in which haemoglobin does not function properly"
      ],
      "id": "en-haemoglobinopathy-en-noun-D3OLiMRd",
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        "(British spelling, medicine) Any of a group of inherited disorders in which haemoglobin does not function properly"
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      "tags": [
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    },
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      "ipa": "/ˌhiməˌɡloʊbɪˈnɑpəθi/",
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  "word": "haemoglobinopathy"
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      "name": "af"
    }
  ],
  "etymology_text": "From haemoglobin + -o- + -pathy.",
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    {
      "form": "haemoglobinopathies",
      "tags": [
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  ],
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    {
      "args": {
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        "English terms suffixed with -pathy",
        "English terms with IPA pronunciation",
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        "Rhymes:English/ɒpəθi/7 syllables",
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        {
          "ref": "1996 December 7, Geoffrey Pasvol, “Malaria and resistance genes—they work in wondrous ways”, in The Lancet, volume 348, number 9041, →DOI, page 1533",
          "text": "Simpler tools for detecting sickle haemoglobin made analysis of the malaria hypothesis in the context of this haemoglobinopathy that much easier, which has facilitated measurement of the trait against a spectrum of endpoints of protection, such as the infection itself, parasite density in infection, uncomplicated disease, and severe disease, and death.",
          "type": "quotation"
        },
        {
          "ref": "2000 February 29, Joseph Telfair, Marilyn Gardner, “Adolescents with Sickle Cell Disease: Determinants of Support Group Attendance and Satisfaction”, in Health & Social Work, →DOI, page 44",
          "text": "Active group membership was operationalized as having attended at least one group meeting during the past year, requesting voluntary inclusion on the group’s roster, and having been formally diagnosed with SCD or a related hemoglobinopathy.",
          "type": "quotation"
        },
        {
          "ref": "2016 December 19, Emmanuel Bissé et al., “Hemoglobin Kirklareli (α H58L), a New Variant Associated with Iron Deficiency and Increased CO Binding”, in Journal of Biological Chemistry, →DOI, page 2548",
          "text": "The clinical phenotypes of over 125 different hemoglobinopathies were interpreted in terms of structural alterations in globin structure.",
          "type": "quotation"
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    {
      "ipa": "/ˌhiːməˌɡləʊbɪˈnɒpəθi/",
      "tags": [
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      ]
    },
    {
      "ipa": "/ˌhiməˌɡloʊbɪˈnɑpəθi/",
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}

This page is a part of the kaikki.org machine-readable All languages combined dictionary. This dictionary is based on structured data extracted on 2024-05-31 from the enwiktionary dump dated 2024-05-02 using wiktextract (91e95e7 and db5a844). The data shown on this site has been post-processed and various details (e.g., extra categories) removed, some information disambiguated, and additional data merged from other sources. See the raw data download page for the unprocessed wiktextract data.

If you use this data in academic research, please cite Tatu Ylonen: Wiktextract: Wiktionary as Machine-Readable Structured Data, Proceedings of the 13th Conference on Language Resources and Evaluation (LREC), pp. 1317-1325, Marseille, 20-25 June 2022. Linking to the relevant page(s) under https://kaikki.org would also be greatly appreciated.