has material basis in germline mutation in MNX1 syndromic disease reproductive system disorder Currarino triad https://github.com/monarch-initiative/mondo/issues/4948 https://github.com/monarch-initiative/mondo/issues/6751 https://github.com/monarch-initiative/mondo/issues/6753 https://github.com/monarch-initiative/mondo/issues/6877 https://www.malacards.org/card/currarino_syndrome MESH:C536221 partial sacral agenesis with intact first sacral vertebra, presacral mass and anorectal malformation GARD:0001626 ICD9:759.89 SCTID:413936007 Currarino triad Currarino syndrome (CS) is a rare congenital disease characterized by the triad of anorectal malformations (ARMs) (usually anal stenosis), presacral mass (commonly anterior sacral meningocele (ASM) or teratoma) and sacral anomalies (i.e. total or partial agenesis of the sacrum and coccyx or deformity of the sacral vertebrae). DOID:0111546 OMIM:176450 icd11.foundation:1532133816 Orphanet:1552 UMLS:C1531773 Currarino syndrome MEDGEN:323460 MONDO:0008305 skeletal dysplasia dysostosis