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 InternationalCreative Commons License
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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