MeSH Browser

MeSH Supplementary: Stratton-Parker Syndrome
Unique ID: C566105
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566105
Entry Term(s): Growth Hormone Deficiency with Wormian Bones, Cardiac Anomaly, and Brachycamptodactyly
Heading Mapped to: *Anus, Imperforate; *Heart Defects, Congenital; *Hypospadias; Growth Hormone / deficiency; *Limb Deformities, Congenital
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Stratton-Parker Syndrome MeSH Supplementary Concept Data 2024