Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
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Preferred Name

NEUTROPHIL IMMUNODEFICIENCY SYNDROME
ID

http://purl.bioontology.org/ontology/OMIM/608203
cui

C1842398
Gene Locus

22q12.3-q13.2
Gene Symbol

RAC2
MIMTYPEMEANING

Phenotype description, molecular basis known.
notation

608203
OMIM Entry Type

3
OMIM MimType Value

pound
prefLabel

NEUTROPHIL IMMUNODEFICIENCY SYNDROME
tui

T047
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Delete Mapping To Ontology Source
http://purl.bmicc.cn/ontology/ICD11CN/4A00.00 International Classification of Diseases, 11th Edition, China LOOM
http://purl.bioontology.org/ontology/MESH/C564275 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C564275 Medical Subject Headings LOOM