MeSH Browser

MeSH Supplementary: Pointer syndrome
Unique ID: C536323
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536323
Entry Term(s): Skeletal abnormalities, camptodactyly, facial anomalies, and feeding difficulties
Registry Number: 0
Heading Mapped to: *Abnormalities, Multiple; *Feeding and Eating Disorders; *Bone Diseases, Developmental; *Limb Deformities, Congenital; *Craniofacial Abnormalities
Frequency: 2
Date of Entry: 2010/08/25
Revision Date: 2016/07/07

Pointer syndrome MeSH Supplementary Concept Data 2024