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Disease Ontology Browser
Laron syndrome (DOID:9521)
Alliance: disease page
Synonyms: Laron-type isolated somatotropin defect
Alt IDs: OMIM:262500, ICD10CM:E34.321, MESH:D046150, NCI:C130994, ORDO:633, UMLS_CUI:C0271568
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.

Disease References using Mouse Models (4)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory