Global Variome shared LOVD

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Phenotype #0000323720 Individual ID 00433188 Associated disease thalalpa Phenotype details microcytic and hypochromic anemia, with reduced mean corpuscular volume (MCV), and mean corpuscular hemoglobin (MCH), level of HbA2 (0.0027) Diagnosis/Initial alpha thalassemia 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 International Created by Johan den Dunnen Date created 2023-03-02 21:40:19 +01:00 (CET) Date last edited 2023-03-03 08:22:08 +01:00 (CET)

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