Phenotype #0000158959

Individual ID 00210394
Associated disease GKD
Phenotype details hypotonia, developmental delay; 14m-febrile seizure; fibroblast GK 5.55%
Diagnosis/Initial glycerol kinase deficiency
Inheritance Unknown
Diagnosis/Definite GKD
Age/Examination -
Age/Diagnosis -
Age/Onset 5d
Phenotype/Onset glyceroluria
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2009-10-16 21:02:19 +02:00 (CEST)
Date last edited 2013-02-01 19:44:12 +01:00 (CET)

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