Medical entity reference · Endocrinology
Laron syndrome
Wikidata · Retrieved 2026-10-13
Congenital disorder characterized by marked short stature associated with normal or high serum growth hormone (GH) and low serum insulin-like growth factor-1 (IGF-I) levels which fail to rise after exogenous GH administration. Wikidata entity Q669822; linked MeSH descriptor D046150. Includes multilingual names and external identifier mappings.
Reference details
- Wikidata entity
- Q669822
- Revision
- 2535728712
- MeSH
- D046150
- OMIM
- 262500
- Disease Ontology
- DOID:9521
- UMLS
- C0271568
Entity description
congenital disorder characterized by marked short stature associated with normal or high serum growth hormone (GH) and low serum insulin-like growth factor-1 (IGF-I) levels which fail to rise after exogenous GH administration
Names in different languages
en: Laron syndrome
zh: 拉伦综合征
zh-hans: 侏儒综合征
ja: ラロン症候群
es: Síndrome de Laron
fr: syndrome de Laron
de: Laron-Syndrom
pt: Síndrome de Laron
ar: متلازمة لارون
ru: Синдром Ларона
English alternative names
Laron-type isolated somatotropin defect (disorder)
Laron-type isolated somatotropin defect
Growth Hormone Receptor Deficiency
Primary growth hormone resistance
Laron-type dwarfism
Pituitary Dwarfism 2
Growth Hormone Insensitivity Syndrome
Primary GH insensitivity
Short stature due to growth hormone resistance
Complete growth hormone insensitivity
Primary GH resistance
GH receptor deficiency
Primary growth hormone insensitivity
Identifier mapping
MeSH: D046150
OMIM: 262500
Disease Ontology: DOID:9521
UMLS: C0271568
Sources and reuse
Structured entity record with names and identifiers. Check individual statements and references at the source.
Source date: 2026-08-24T08:09:28Z. Retrieved: 2026-10-13. Text has been organized for reading; this import has not been independently reviewed by a clinician. It is not individualized medical advice.