See Bardet-Biedl syndrome on Wiktionary
{
"etymology_text": "Named after Georges Bardet and Arthur Biedl.",
"head_templates": [
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"expansion": "Bardet-Biedl syndrome",
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"lang_code": "en",
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{
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{
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"coordinate_terms": [
{
"word": "Alström syndrome"
},
{
"word": "Laurence-Moon syndrome"
},
{
"word": "LMS"
},
{
"word": "McKusick-Kaufman syndrome"
},
{
"word": "MKS"
},
{
"word": "MKKS"
},
{
"word": "MORM syndrome"
},
{
"word": "Usher syndrome"
}
],
"derived": [
{
"word": "BBS"
},
{
"word": "BBSome"
}
],
"glosses": [
"A ciliopathic human genetic disorder characterized principally by obesity, retinitis pigmentosa, polydactyly, hypogonadism, and renal failure in some cases."
],
"hypernyms": [
{
"english": "no longer a valid classification",
"tags": [
"historical"
],
"word": "Laurence-Moon-Bardet-Biedl syndrome"
}
],
"id": "en-Bardet-Biedl_syndrome-en-name-O569xHsm",
"links": [
[
"ciliopathic",
"ciliopathic"
],
[
"human",
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],
[
"genetic",
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],
[
"disorder",
"disorder"
],
[
"obesity",
"obesity"
],
[
"retinitis pigmentosa",
"retinitis pigmentosa"
],
[
"polydactyly",
"polydactyly"
],
[
"hypogonadism",
"hypogonadism"
],
[
"renal",
"renal"
],
[
"failure",
"failure"
]
],
"synonyms": [
{
"word": "BBS"
}
],
"translations": [
{
"code": "fr",
"lang": "French",
"sense": "Translations",
"tags": [
"masculine"
],
"word": "syndrome de Bardet-Biedl"
}
],
"wikipedia": [
"Arthur Biedl",
"Bardet-Biedl syndrome",
"Georges Bardet"
]
}
],
"word": "Bardet-Biedl syndrome"
}
{
"coordinate_terms": [
{
"word": "Alström syndrome"
},
{
"word": "Laurence-Moon syndrome"
},
{
"word": "LMS"
},
{
"word": "McKusick-Kaufman syndrome"
},
{
"word": "MKS"
},
{
"word": "MKKS"
},
{
"word": "MORM syndrome"
},
{
"word": "Usher syndrome"
}
],
"derived": [
{
"word": "BBS"
},
{
"word": "BBSome"
}
],
"etymology_text": "Named after Georges Bardet and Arthur Biedl.",
"head_templates": [
{
"args": {},
"expansion": "Bardet-Biedl syndrome",
"name": "en-proper noun"
}
],
"hypernyms": [
{
"english": "no longer a valid classification",
"tags": [
"historical"
],
"word": "Laurence-Moon-Bardet-Biedl syndrome"
}
],
"lang": "English",
"lang_code": "en",
"pos": "name",
"senses": [
{
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"Pages with entries",
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"Translation table header lacks gloss"
],
"glosses": [
"A ciliopathic human genetic disorder characterized principally by obesity, retinitis pigmentosa, polydactyly, hypogonadism, and renal failure in some cases."
],
"links": [
[
"ciliopathic",
"ciliopathic"
],
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"human",
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],
[
"genetic",
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],
[
"disorder",
"disorder"
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[
"obesity",
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],
[
"retinitis pigmentosa",
"retinitis pigmentosa"
],
[
"polydactyly",
"polydactyly"
],
[
"hypogonadism",
"hypogonadism"
],
[
"renal",
"renal"
],
[
"failure",
"failure"
]
],
"wikipedia": [
"Arthur Biedl",
"Bardet-Biedl syndrome",
"Georges Bardet"
]
}
],
"synonyms": [
{
"word": "BBS"
}
],
"translations": [
{
"code": "fr",
"lang": "French",
"sense": "Translations",
"tags": [
"masculine"
],
"word": "syndrome de Bardet-Biedl"
}
],
"word": "Bardet-Biedl syndrome"
}
Download raw JSONL data for Bardet-Biedl syndrome meaning in All languages combined (1.7kB)
This page is a part of the kaikki.org machine-readable All languages combined dictionary. This dictionary is based on structured data extracted on 2025-01-25 from the enwiktionary dump dated 2025-01-20 using wiktextract (c15a5ce and 5c11237). 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.