MeSH Browser

MeSH Supplementary: Chromosome 2q37 deletion syndrome
Unique ID: C538317
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538317
Entry Term(s): 2q37 deletion syndrome; Albright hereditary osteodystrophy-like syndrome; Brachydactyly-Mental Retardation syndrome; Chromosome 2, monosomy 2q37; Deletion 2q37; Monosomy 2q37
Registry Numbers: 0
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 2
Frequency: 26
Date of Entry: 2010/08/25
Revision Date: 2013/10/24

Chromosome 2q37 deletion syndrome MeSH Supplementary Concept Data 2024