Phenotype #0000122513

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00150111
Associated disease	IMD104
Phenotype details	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	00y09m (9 months)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Sinem Firtina
Database submission license	No license selected
Created by	Sinem Firtina
Date created	2018-01-10 10:04:43 +01:00 (CET)
Date last edited	2018-01-13 11:55:43 +01:00 (CET)

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