Phenotype #0000325672

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00435485
Associated disease	IMD
Phenotype details	severe combined immunodeficiency, sensitivity to ionizing radiation, no microcephaly, mild developmental delay
Diagnosis/Initial	-
Inheritance	Unknown
Diagnosis/Definite	-
Age/Examination	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2023-08-03 09:54:29 +02:00 (CEST)
Date last edited	N/A

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