Phenotype #0000087501

Individual ID 00111415
Associated disease ID
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Isolated (sporadic)
Phenotype details Mild ID, obesity, normal growth, several fractures, hypertonia lower limbs, movement anomalies; mild intellectual disability (HP:0001256); mild global developmental delay (HP:0011342)
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 2017-08-03 07:55:03 +02:00 (CEST)
Date last edited 2020-05-12 12:33:06 +02:00 (CEST)

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