Phenotype #0000084330

Individual ID 00106517
Associated disease MRT
Phenotype details Developmental delay/Intellectual disability, Speech/language delay Motor delay, Hypotonia, Microcephaly
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination 02y01m (2 years, 1 month)
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 21:00:27 +02:00 (CEST)
Date last edited N/A

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