Global Variome shared LOVD

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Phenotype #0000093192 Individual ID 00117727 Associated disease HPE11 Phenotype details agenesis of corpus callosum, hypotelorism, growth hormone deficiency, global developmental delay; dark, thick eyebrows with synophrys Diagnosis/Initial - Inheritance Unknown 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 International Created by Gerard C.P. Schaafsma Date created 2011-08-17 13:53:31 +02:00 (CEST) Date last edited N/A

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