Phenotype #0000323581

Individual ID 00433055
Associated disease IMD
Phenotype details combined immunodeficiency (not SCID), selective T cell deficiency
Diagnosis/Initial primary immunodeficiency disease
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 13y (13 years)
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 2023-02-28 15:41:53 +01:00 (CET)
Date last edited N/A

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