MeSH Browser

MeSH Supplementary: Short Stature, Idiopathic, Autosomal
Unique ID: C565805
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565805
Entry Term(s): Growth Hormone Deficiency, Isolated, Partial; Growth Hormone, Insensitivity To, Partial
Registry Number: 0
Heading Mapped to: *Dwarfism, Pituitary
Frequency: 21
Note: A hereditary autosomal recessive conditon resulting in short stature due to mutations in the GHSR gene. OMIM: 600946.0006
Date of Entry: 2012/11/05
Revision Date: 2015/11/10

Short Stature, Idiopathic, Autosomal MeSH Supplementary Concept Data 2024