Phenotype #0000060088

Individual ID 00080524
Associated disease XLP1
Phenotype details Symptoms: Classical XLP; hypogammaglobulinemia
Diagnosis/Initial -
Inheritance Familial, X-linked recessive
Diagnosis/Definite -
Age/Examination 56y (56 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Gerard C.P. Schaafsma
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Gerard C.P. Schaafsma
Date created 2000-01-12 00:00:00 +01:00 (CET)
Date last edited 2001-10-03 00:00:00 +02:00 (CEST)

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