Phenotype #0000106399

Individual ID 00133649
Associated disease ID
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Isolated (sporadic)
Phenotype details severe intellectual disability (HP:0010864); severe global developmental delay (HP:0011344); severe speech delay (HP:0000750)
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Bernt Popp
Database submission license No license selected
Created by Bernt Popp
Date created 2017-11-16 11:43:02 +01:00 (CET)
Date last edited 2020-05-12 12:33:06 +02:00 (CEST)

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