Bardet-Biedl syndrome
ciliopathic human genetic disorder that produces many effects and affects many body systems
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Bardet-Biedl syndrome
Summary
Bardet-Biedl syndrome is a rare disease[1]. It draws 1,025 Wikipedia views per month (rare_disease category, ranking #126 of 627).[2]
Key Facts
- Bardet-Biedl syndrome's instance of is recorded as rare disease[3].
- Bardet-Biedl syndrome's instance of is recorded as class of disease[4].
- Arthur Biedl is named after Bardet-Biedl syndrome[5].
- Bardet-Biedl syndrome is a type of autosomal recessive disease[6].
- Bardet-Biedl syndrome is a type of syndromic obesity[7].
- Bardet-Biedl syndrome is a type of disease[8].
- Bardet-Biedl syndrome's Commons category is recorded as Bardet–Biedl syndrome[9].
- Bardet-Biedl syndrome's NCI Thesaurus ID is recorded as C118632[10].
- Bardet-Biedl syndrome's health specialty is recorded as medical genetics[11].
- Bardet-Biedl syndrome's genetic association is recorded as BBS1[12].
- Bardet-Biedl syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_1935[13].
- Bardet-Biedl syndrome's exact match is recorded as http://identifiers.org/doid/DOID:1935[14].
- Bardet-Biedl syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_110[15].
- Bardet-Biedl syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
Bardet-Biedl syndrome draws 1,025 Wikipedia views per month (rare_disease category, ranking #126 of 627).[2] It has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[17]