Phenotype #0000017579

Individual ID 00019839
Associated disease ID
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Isolated (sporadic)
Phenotype details developmental delay, no major dysmorphisms, no ocular anomalies, no pituitary deficiency
Age/Examination ?
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Marianne Vos (LOVD-team)
Database submission license No license selected
Created by Marianne Vos (LOVD-team)
Date created 2014-09-02 12:50:21 +02:00 (CEST)
Date last edited 2014-11-07 20:10:04 +01:00 (CET)

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