FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Laron syndrome ID (Ontology) DOID:9521 (Human Disease)
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.
Also Known As "Laron-type isolated somatotropin defect"
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autosomal genetic disease
 |__autosomal recessive disease__
disease                          |
 |__syndrome_____________________|
                                 Laron syndrome
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Is a autosomal recessive disease
syndrome
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Synonyms
  • "Laron-type isolated somatotropin defect" EXACT
Secondary IDs
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GARD:6859
ICD10CM:E34.321
MESH:D046150
MIM:262500
NCI:C130994
ORDO:633
SNOMEDCT_US_2023_03_01:38196001
UMLS_CUI:C0271568