Phenotype #0000087485

Individual ID 00111400
Associated disease PTHS
Phenotype details Hypotonia, developmental delay
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
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 01:10:53 +02:00 (CEST)
Date last edited 2017-08-04 09:29:30 +02:00 (CEST)

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