Larsen syndrome
autosomal dominant disease that is characterized by large-joint dislocations and characteristic craniofacial abnormalities
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Larsen syndrome
Summary
Larsen syndrome is a head and neck disease[1]. It draws 476 Wikipedia views per month (head_and_neck_disease category, ranking #35 of 92).[2]
Key Facts
- Larsen syndrome's instance of is recorded as head and neck disease[3].
- Larsen syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- Larsen syndrome's instance of is recorded as rare disease[5].
- Larsen syndrome's instance of is recorded as class of disease[6].
- Larsen syndrome is a type of autosomal dominant disease[7].
- Larsen syndrome is a type of filamin-related bone disorder[8].
- Larsen syndrome is a type of primary bone dysplasia with multiple joint dislocations[9].
- Larsen syndrome is a type of rare developmental defect with connective tissue involvement[10].
- Larsen syndrome is a type of orofacial clefting syndrome[11].
- Larsen syndrome's Commons category is recorded as Larsen syndrome[12].
- Larsen syndrome's ICD-9-CM is recorded as 759.89[13].
- Larsen syndrome's different from is recorded as postpericardiotomy syndrome[14].
- Larsen syndrome's genetic association is recorded as FLNB[15].
- Larsen syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14764[16].
- Larsen syndrome's exact match is recorded as http://identifiers.org/doid/DOID:14764[17].
- Larsen syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_503[18].
- Larsen syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
Why It Matters
Larsen syndrome draws 476 Wikipedia views per month (head_and_neck_disease category, ranking #35 of 92).[2] It has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[20] It is known by 19 alternative names across languages and contexts.[21]