Short Stature, Idiopathic, Autosomal [Supplementary Concept]
A hereditary autosomal recessive conditon resulting in short stature due to mutations in the GHSR gene. OMIM: 600946.0006
Date introduced: November 5, 2012
MeSH Unique ID: C565805
Heading Mapped to:
Entry Terms:
- Growth Hormone Deficiency, Isolated, Partial
- Growth Hormone, Insensitivity To, Partial