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    "__licence": {
      "identifier": "CC-BY-4.0",
      "link": "https://creativecommons.org/licenses/by/4.0",
      "name": "Creative Commons Attribution 4.0 International"
    },
    "results": {
      "Date": "2026-06-23 07:53:50",
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          "Label": null,
          "Value": 1
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      "DisorderGroup": "Disorder",
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          "DisorderMappingICDRefUrl": null,
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          "DisorderMappingRelation": "E (Exact mapping: the two concepts are equivalent)",
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          "Source": "GARD"
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          "DisorderMappingICDRefUrl": null,
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          "DisorderMappingRelation": "NTBT (ORPHAcode is narrower than the targeted code used to represent it)",
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          "Reference": "Q38.0",
          "Source": "ICD-10"
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          "DisorderMappingICDRefUrl": "https://icd.who.int/browse/latest-release/mms/en#1106405864%2fother",
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          "Source": "MONDO"
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          "DisorderMappingValidationStatus": "Validated",
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          "Source": "MeSH"
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          "DisorderMappingICDRefUrl": null,
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          "Source": "OMIM"
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          "DisorderMappingICDRefUrl": null,
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          "Source": "OMIM"
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          "DisorderMappingICDRefUrl": null,
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          "DisorderMappingICDRefUrl": null,
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      "OrphanetURL": "http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=888",
      "Preferred term": "Van der Woude syndrome",
      "SummaryInformation": [
        {
          "Definition": "Van der Woude syndrome (VWS) is a rare congenital genetic dysmorphic syndrome characterized by paramedian lower-lip fistulae, cleft lip with or without cleft palate, or isolated cleft palate."
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        "Cleft lip/palate with mucous cysts of lower lip",
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      "Typology": "Malformation syndrome"
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    "query": {}
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