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Laron syndrome

Disease Summary
Associated Targets (3)
Tclin

2

Tbio

1


GARD Rare
Mondo Description Laron syndrome is a 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.
Uniprot Description A severe form of growth hormone insensitivity characterized by growth impairment, short stature, dysfunctional growth hormone receptor, and failure to generate insulin-like growth factor I in response to growth hormone.
Mondo Term and Equivalent IDs
MONDO:0009877:  Laron syndrome
GARD:0006859: 
MESH:D046150: 
NCIT:C130994: 
Orphanet:633: 
SCTID:38196001: