Phenotype #0000046706

Individual ID 00060216
Associated disease NAGSD
Phenotype details poor feeding, seizures, lethargy
younger sibling: NCG-treated before symptoms developed
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 00y00m02d
Phenotype/Onset -
Protein -
Owner name Johannes Häberle
Database submission license No license selected
Created by Johannes Häberle
Date created 2016-03-11 14:57:52 +01:00 (CET)
Date last edited 2019-07-20 20:25:58 +02:00 (CEST)

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