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

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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