radioulnar synostosis

Summary

radioulnar synostosis is a developmental defect during embryogenesis^[1]. It draws 171 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's subclass of is recorded as synostosis^[5].
• radioulnar synostosis's subclass of is recorded as joint formation defects^[6].
• radioulnar synostosis's subclass of is recorded as congenital disorder^[7].
• radioulnar synostosis's subclass of is recorded as disease^[8].
• radioulnar synostosis's MeSH descriptor ID is recorded as C562408^[9].
• radioulnar synostosis's OMIM ID is recorded as 179300^[10].
• radioulnar synostosis's Disease Ontology ID is recorded as DOID:9827^[11].
• radioulnar synostosis's Orphanet ID is recorded as 3269^[12].
• radioulnar synostosis's ICD-9-CM is recorded as 755.53^[13].
• radioulnar synostosis's health specialty is recorded as medical genetics^[14].
• radioulnar synostosis's genetic association is recorded as SMAD6^[15].
• radioulnar synostosis's exact match is recorded as http://purl.obolibrary.org/obo/DOID_9827^[16].
• radioulnar synostosis's exact match is recorded as http://identifiers.org/doid/DOID:9827^[17].
• radioulnar synostosis's exact match is recorded as http://purl.obolibrary.org/obo/HP_0002974^[18].
• radioulnar synostosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3269^[19].
• radioulnar synostosis's UMLS CUI is recorded as C0431795^[20].
• radioulnar synostosis's UMLS CUI is recorded as C0158761^[21].
• radioulnar synostosis's UMLS CUI is recorded as C5679809^[22].
• radioulnar synostosis's Human Phenotype Ontology ID is recorded as HP:0002974^[23].
• radioulnar synostosis's ICD-10-CM is recorded as Q74.0^[24].
• radioulnar synostosis's GARD rare disease ID is recorded as 10876^[25].
• radioulnar synostosis's on focus list of Wikimedia project is recorded as WikiProject Medicine^[26].
• radioulnar synostosis's Mondo ID is recorded as MONDO_0017985^[27].

Why It Matters

radioulnar synostosis draws 171 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.^[28] It is known by 3 alternative names across languages and contexts.^[29]