Phenotype #0000059452

Individual ID 00079741
Associated disease Laron
Phenotype details Laron syndrome; LTD; slow physical and mental development, clinical features of GH deficiency (with high GH levels and low IGF-1 levels); no serum GH binding protein detected; no 125I labeled GH binding detected in liver microsomal membranes
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2008-09-19 15:40:07 +02:00 (CEST)
Date last edited 2009-08-21 17:15:48 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.