MeSH Browser

MeSH Supplementary: Pseudotrisomy 13 syndrome
Unique ID: C535829
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535829
Entry Term(s): Holoprosencephaly polydactyly syndrome; Holoprosencephaly-Polydactyly Syndrome; Pseudo trisomy 13 syndrome
Heading Mapped to: Chromosomes, Human, Pair 13; *Fetal Macrosomia; *Hand Deformities, Congenital; *Trisomy; *Holoprosencephaly; *Polydactyly
Frequency: 5
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Pseudotrisomy 13 syndrome MeSH Supplementary Concept Data 2024