Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Neutrophil Immunodeficiency Syndrome
ID

http://purl.bioontology.org/ontology/MESH/C564275
cui

C1842398
HM

D007153
Inverse of RB

0
Mapped to

http://purl.bioontology.org/ontology/MESH/D007153
MDA

20121105
MeSH Frequency

0
notation

C564275
prefLabel

Neutrophil Immunodeficiency Syndrome
SC

3
Scope Statement

mutation in RAC2 gene of NAPDH oxidase
TERMUI

T804528
TH

OMIM (2013)
tui

T047
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/608203 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/608203 Online Mendelian Inheritance in Man LOOM
http://purl.bmicc.cn/ontology/ICD11CN/4A00.00 International Classification of Diseases, 11th Edition, China LOOM
http://purl.bioontology.org/ontology/OMIM/602049 Online Mendelian Inheritance in Man CUI