Phenotype #0000083832

Individual ID 00105924
Associated disease HML
Phenotype details lifelong exercise intolerance, symptoms muscle fatigue, shortness of breath, tachycardia with minor levels physical exertion with episodes myoglobinuria; low work/oxidative capacity, deficiency succinate dehydrogenase/aconitase
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
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 2010-03-20 19:04:27 +01:00 (CET)
Date last edited 2012-03-09 18:26:59 +01:00 (CET)