MeSH Browser

MeSH Supplementary: Sacral Agenesis Syndrome
Unique ID: C566762
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566762
Entry Term(s): Sacral Agenesis, Hereditary, With Presacral Mass, Anterior Meningocele, And-Or Teratoma, And Anorectal Malformation
Registry Numbers: 0
Heading Mapped to: Anal Canal / abnormalities; *Meningocele; Rectum / abnormalities; Sacrum / abnormalities; *Teratoma
Frequency: 3
Note: mutations in MNX1
Date of Entry: 2012/11/05
Revision Date: 2015/11/11

Sacral Agenesis Syndrome MeSH Supplementary Concept Data 2025