MeSH Browser

MeSH Supplementary: Chromosome 3, monosomy 3p
Unique ID: C536804
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536804
Entry Term(s): Chromosome 3, deletion 3p; Deletion 3p; Monosomy 3p
Registry Number: 0
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 3
Frequency: 33
Note: Deletion of the distal portion of the short arm (p) of chromosome 3 may result in a range of abnormalities that vary in severity. Among the more common are prenatal and postnatal growth deficiency; severe intellectual disability; craniofacial abnormalities; eyebrows that grow together (synophrys), HYPERTRICHOSIS; and POLYDACTYLY. OMIM: 613792
Date of Entry: 2010/08/25
Revision Date: 2016/08/01

Concept UI: M0531265
Registry Number: 0
Terms: Chromosome 3, monosomy 3p Preferred Term
Term UI T740490
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Chromosome 3, deletion 3p
Term UI T740492
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Deletion 3p
Term UI T740493
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010); Monosomy 3p
Term UI T740491
Date02/24/2009
LexicalTag NON
ThesaurusID ORD (2010)

Chromosome 3, monosomy 3p MeSH Supplementary Concept Data 2023