MeSH Browser

MeSH Supplementary: Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence
Unique ID: C563127
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563127
Entry Term(s): Toriello-Carey Syndrome
Heading Mapped to: *Heart Defects, Congenital; *Pierre Robin Syndrome; *Urogenital Abnormalities; *Limb Deformities, Congenital; *Craniofacial Abnormalities; *Agenesis of Corpus Callosum
Frequency: 5
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence MeSH Supplementary Concept Data 2024