Laron syndrome

Summary

DOID:9521 - Laron syndrome

Disease Ontology 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.

Synonyms: Laron-type isolated somatotropin defect, Laron-type isolated somatotropin defect (disorder),

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: ghr

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009877 - Laron syndrome

MONDO:0009877 - Laron syndrome

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), syndrome (is_a)