Disease #02744 (IMD73A (immunodeficiency, type 73A, with defective neutrophil chemotaxix and leukocytosis), OMIM:608203)

Official abbreviation IMD73A
Name immunodeficiency, type 73A, with defective neutrophil chemotaxix and leukocytosis
OMIM ID 608203
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 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-07-29 11:51:53 +02:00 (CEST)

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