Disease #06948 (IMD73B (immunodeficiency, type 73B, with defective neutrophil chemotaxis and lymphopenia), OMIM:618986)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	IMD73B
Name	immunodeficiency, type 73B, with defective neutrophil chemotaxis and lymphopenia
OMIM ID	618986
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RAC2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-07-29 11:52:45 +02:00 (CEST)
Date last edited	N/A

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