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Pseudotrisomy 13 syndrome MeSH Supplementary Concept Data 2024


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
Registry Number
0
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 Preferred
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