Currarino syndrome
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Currarino syndrome
Summary
Currarino syndrome is a developmental defect during embryogenesis[1]. It draws 39 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #99 of 308).[2]
Key Facts
- Currarino syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Currarino syndrome's instance of is recorded as rare disease[4].
- Currarino syndrome's instance of is recorded as class of disease[5].
- Currarino syndrome's subclass of is recorded as dysostosis[6].
- Currarino syndrome's subclass of is recorded as syndromic anorectal malformation[7].
- Currarino syndrome's subclass of is recorded as syndromic uterovaginal malformation[8].
- Currarino syndrome's subclass of is recorded as rare genetic gynecological and obstetrical diseases[9].
- Currarino syndrome's subclass of is recorded as dysostosis with predominant vertebral and costal involvement[10].
- Currarino syndrome's subclass of is recorded as autosomal dominant disease[11].
- Currarino syndrome's subclass of is recorded as syndrome[12].
- Currarino syndrome's MeSH descriptor ID is recorded as C536221[13].
- Currarino syndrome's OMIM ID is recorded as 176450[14].
- Currarino syndrome's DiseasesDB is recorded as 33509[15].
- Currarino syndrome's Freebase ID is recorded as /m/02pzgq8[16].
- Currarino syndrome's KEGG ID is recorded as H00463[17].
- Currarino syndrome's Disease Ontology ID is recorded as DOID:0111546[18].
- Currarino syndrome's Orphanet ID is recorded as 1552[19].
- Currarino syndrome's ICD-9-CM is recorded as 759.89[20].
- Currarino syndrome's genetic association is recorded as MNX1[21].
- Currarino syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1552[22].
- Currarino syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111546[23].
- Currarino syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111546[24].
- Currarino syndrome's UMLS CUI is recorded as C1867775[25].
- Currarino syndrome's UMLS CUI is recorded as C1415596[26].
- Currarino syndrome's UMLS CUI is recorded as C1867774[27].
Why It Matters
Currarino syndrome draws 39 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #99 of 308).[2] It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[28] It is known by 10 alternative names across languages and contexts.[29]