Phenotype #0000144727

Individual ID 00184597
Associated disease CCDS3;GATMD
Diagnosis/Initial GAMT deficiency
Diagnosis/Definite CCDS-3
Phenotype details -
Inheritance Familial, autosomal recessive
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Rahma MANI
Database submission license No license selected
Created by Gajja Salomons
Date created 2016-08-30 16:36:34 +02:00 (CEST)
Date last edited N/A

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