dipygus

Summary

dipygus is a developmental defect during embryogenesis^[1]. dipygus draws 172 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #37 of 308).^[2]

Key Facts

• dipygus's image is recorded as Myrtle Corbin.jpg^[3].
• dipygus's instance of is recorded as developmental defect during embryogenesis^[4].
• dipygus's instance of is recorded as rare disease^[5].
• dipygus's instance of is recorded as class of disease^[6].
• dipygus's subclass of is recorded as genetic nervous system disorder^[7].
• dipygus's subclass of is recorded as other syndrome with a central nervous system malformation as major feature^[8].
• dipygus's subclass of is recorded as syndromic anorectal malformation^[9].
• dipygus's subclass of is recorded as Caudal duplication^[10].
• dipygus's MeSH descriptor ID is recorded as C564315^[11].
• dipygus's OMIM ID is recorded as 607864^[12].
• dipygus's KEGG ID is recorded as H00934^[13].
• dipygus's Orphanet ID is recorded as 1756^[14].
• dipygus's genetic association is recorded as AXIN1^[15].
• dipygus's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1756^[16].
• dipygus's UMLS CUI is recorded as C0544738^[17].
• dipygus's UMLS CUI is recorded as C1842884^[18].
• dipygus's UMLS CUI is recorded as C0266688^[19].
• dipygus's ICD-10-CM is recorded as Q87.8^[20].
• dipygus's GARD rare disease ID is recorded as 1164^[21].
• dipygus's Mondo ID is recorded as MONDO_0011928^[22].
• dipygus's Microsoft Academic ID is recorded as 2780862463^[23].
• dipygus's UniProt disease ID is recorded as DI-02877^[24].

Why It Matters

dipygus draws 172 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #37 of 308).^[2] dipygus has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.^[25] dipygus is known by 5 alternative names across languages and contexts.^[26]