Talk:Q669822
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Autodescription — Laron syndrome (Q669822)
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
- Useful links:
- View it! – Images depicting the item on Commons
- Report on constraint conformation of “Laron syndrome” claims and statements. Constraints report for items data
For help about classification, see Wikidata:Classification.
- Parent classes (classes of items which contain this one item)
- Laron syndrome (Q669822)
- autosomal recessive disease (Q10267817)
- growth hormone insensitivity syndrome (Q47455810)
- syndrome (Q179630)
- Laron syndrome (Q669822)
- Subclasses (classes which contain special kinds of items of this class)
- ⟨
Laron syndrome⟩ on wikidata tree visualisation (external tool)(depth=1) - Generic queries for classes
- See also
- This documentation is generated using
{{Item documentation}}.
Why not show the Orphanet ID as shown in the Wikipedia article?[edit]
Why not show the Orphanet ID 633 for Laron syndrome as shown in the Wikipedia article?