Phenotype #0000069521

Individual ID 00090179
Associated disease -
Phenotype details methemoglobinemia type I; see paper ..., all carriers have reduced MetHb reductase activity
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 12y (12 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Joaquin Brintrup
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-12-09 15:09:15 +01:00 (CET)
Date last edited 2016-12-10 10:07:53 +01:00 (CET)

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