Currarino syndrome
medical condition
Press Enter · cited answer in seconds
0 sources
Currarino syndrome
Summary
Currarino syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[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 is a type of dysostosis[6].
- Currarino syndrome is a type of syndromic anorectal malformation[7].
- Currarino syndrome is a type of syndromic uterovaginal malformation[8].
- Currarino syndrome is a type of rare genetic gynecological and obstetrical diseases[9].
- Currarino syndrome is a type of dysostosis with predominant vertebral and costal involvement[10].
- Currarino syndrome is a type of autosomal dominant disease[11].
- Currarino syndrome is a type of syndrome[12].
- Currarino syndrome's ICD-9-CM is recorded as 759.89[13].
- Currarino syndrome's genetic association is recorded as MNX1[14].
- Currarino syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1552[15].
- Currarino syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111546[16].
- Currarino syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111546[17].
Why It Matters
Currarino syndrome has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2] It is known by 10 alternative names across languages and contexts.[18]