radioulnar synostosis
Human disease
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radioulnar synostosis
Summary
radioulnar synostosis is a developmental defect during embryogenesis[1]. It draws 372 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #52 of 308).[2]
Key Facts
- radioulnar synostosis's instance of is recorded as developmental defect during embryogenesis[3].
- radioulnar synostosis's instance of is recorded as class of disease[4].
- radioulnar synostosis is a type of synostosis[5].
- radioulnar synostosis is a type of joint formation defects[6].
- radioulnar synostosis is a type of congenital disorder[7].
- radioulnar synostosis is a type of disease[8].
- radioulnar synostosis's ICD-9-CM is recorded as 755.53[9].
- radioulnar synostosis's health specialty is recorded as medical genetics[10].
- radioulnar synostosis's genetic association is recorded as SMAD6[11].
- radioulnar synostosis's exact match is recorded as http://purl.obolibrary.org/obo/DOID_9827[12].
- radioulnar synostosis's exact match is recorded as http://identifiers.org/doid/DOID:9827[13].
- radioulnar synostosis's exact match is recorded as http://purl.obolibrary.org/obo/HP_0002974[14].
- radioulnar synostosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3269[15].
- radioulnar synostosis's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
radioulnar synostosis draws 372 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #52 of 308).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[17] It is known by 3 alternative names across languages and contexts.[18]