Term Name:	Laron syndrome
Synonyms:	Laron-type isolated somatotropin defect
Definition:	A syndrome characterized by marked short stature with normal or high serum growth hormone and low serum insulin-like growth factor-1 levels that has_material_basis_in homozygous or compound heterozygous mutation in GHR on chromosome 5p13-p12.
Ontology:	Human Disease [DOID:9521]   ( DOID:9521 )