Phenotype #0000059443

Individual ID 00079732
Associated disease -
Phenotype details insulin-like growth factor I deficiency; bone age 1.2y delayed; no conspicuous features of Laron syndrome
Diagnosis/Initial -
Inheritance Isolated (sporadic)
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 2009-07-01 13:50:23 +02:00 (CEST)
Date last edited 2009-09-06 10:55:40 +02:00 (CEST)

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