Phenotype #0000084332

Individual ID 00106519
Associated disease ID
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Isolated (sporadic)
Phenotype details mild Developmental delay/Intellectual disability, mild speech/language delay, Motor delay, Large helices of both ears (similar to father),; mild intellectual disability (HP:0001256); mild global developmental delay (HP:0011342); mild speech delay (HP:0000750)
Age/Examination 10y09m (10 years, 9 months)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Bernt Popp
Database submission license No license selected
Created by Bernt Popp
Date created 2017-07-02 21:25:57 +02:00 (CEST)
Date last edited 2020-05-12 12:33:06 +02:00 (CEST)

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