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Pointer syndrome MeSH Supplementary Concept Data 2023


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 Preferred
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