Phenotype #0000015244

Individual ID 00016843
Associated disease HOMG1
Phenotype details initial Mg2+ 0.22 mM, FE Mg2+ 2.6%; age onset 5w
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 00y01m
Phenotype/Onset seizures
Protein -
Owner name Karl Schlingmann
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2014-05-30 14:35:30 +02:00 (CEST)
Date last edited N/A

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