Laron syndrome
type: Thing
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
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  value: growth hormone insensitivity syndrome
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confidence:
  popularity graph score:
    score: 0.017
    score pct: 2
    tier: established
    components:
      sitelinks: 19
      sitelinks norm: 0.045
      unique citations: 10
      unique citations norm: 0.004
      monthly pageviews: 818
      monthly pageviews norm: 0.0
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  unique citations: 10
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  yearly pageviews: 1252
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    pct: 4.5
  tier: established
claims:
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    value label: autosomal recessive disease
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    value label: growth hormone insensitivity syndrome
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    value label: syndrome
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  P493:
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value: DOID:9521
source count: 1
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source count: 0
confidence: 0.0

value: 633
source count: 1
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value: C130994
source count: 1
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value: Q162606
source count: 0
confidence: 0.0
value label: endocrinology

value: Q14907631
source count: 3
confidence: 0.6
value label: GHR

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source count: 1
confidence: 0.2

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source count: 0
confidence: 0.0

value: C0271568
source count: 1
confidence: 0.2

value: Laron-Syndrome
source count: 1
confidence: 0.2

value: laron-syndrome
source count: 0
confidence: 0.0

value: E34.3
source count: 2
confidence: 0.4

value: 6859
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value: Q4099686
source count: 0
confidence: 0.0
value label: WikiProject Medicine

value: MONDO_0009877
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value: 2781430988
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value: laron-syndrome
source count: 0
confidence: 0.0

value: 987007548949505171
source count: 1
confidence: 0.2

value: Larons_syndrom
source count: 0
confidence: 0.0

value: Laron syndrome
source count: 0
confidence: 0.0

value: DI-01877
source count: 0
confidence: 0.0

source count: 0
confidence: 0.0

source: Open Targets Platform
stated in qid: Q113138000
retrieved: 2023-08-24

source: Identifiers.org
stated in qid: Q16335166

retrieved: 2019-04-03

source: Freebase Data Dumps
stated in qid: Q15241312
pub year: 2013

source: Monarch Disease Ontology release 2018-06-29
stated in qid: Q55345445
retrieved: 2018-07-28

source: Disease Ontology
stated in qid: Q5282129
retrieved: 2020-11-30

source: UniProt
stated in qid: Q905695
retrieved: 2019-08-13

source: Diverse growth hormone receptor gene mutations in Laron syndrome.
stated in qid: Q35194129

source: Quora
stated in qid: Q51711

source: National Library of Israel
stated in qid: Q188915

wikidata id: Q669822
domain: rare_disease
level: standard
html url: https://4ort.xyz/entity/laron-syndrome
markdown url: https://4ort.xyz/entity/laron-syndrome.md
facts url summary: https://4ort.xyz/entity/laron-syndrome/facts.json
facts url standard: https://4ort.xyz/entity/laron-syndrome/facts.json
facts url full: https://4ort.xyz/entity/laron-syndrome/facts.json
data source: Wikidata (CC0 / public domain)
license: https://creativecommons.org/publicdomain/zero/1.0/
api version: v1
served at: 2026-08-29T18:06:39.447419Z
entity updated at: 2026-05-03T21:19:00.258443+00:00Z
entity created at: 2026-04-10T23:41:50.734498+00:00Z