International Classification of Diseases, Version 10 - Clinical Modification - Genetic anomalies of leukocytes - Classes

Last uploaded: January 29, 2019

Preferred Name	Genetic anomalies of leukocytes
Synonyms	Pelger-HuÃ«t syndrome
ID	http://purl.bioontology.org/ontology/ICD10CM/D72.0
altLabel	Pelger-HuÃ«t syndrome May-Hegglin syndrome Hereditary leukomelanopathy Hereditary leukocytic hyposegmentation May-Hegglin (granulation) (granulocyte) anomaly Hereditary leukocytic hypersegmentation Alder (granulation) (granulocyte) anomaly Pelger-HuÃ«t (granulation) (granulocyte) anomaly Alder syndrome
cui	C1400046 C0007965 C1400295 C2873816 C0281938 C1527030 C0272184 C0017377 C2873815 C2873814
EXCLUDES1	ChÃ©diak (-Steinbrinck)-Higashi syndrome (E70.330)
Inverse of SIB	http://purl.bioontology.org/ontology/ICD10CM/D72.9 http://purl.bioontology.org/ontology/ICD10CM/D72.1 http://purl.bioontology.org/ontology/ICD10CM/D72.8
notation	D72.0
Order number	03506
prefLabel	Genetic anomalies of leukocytes
tui	T047
subClassOf	http://purl.bioontology.org/ontology/ICD10CM/D72

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/OMIM/214500	Online Mendelian Inheritance in Man	CUI
http://purl.bioontology.org/ontology/ICD10/D72.0	International Classification of Diseases, Version 10	CUI
http://purl.bioontology.org/ontology/ICD10/D72.0	International Classification of Diseases, Version 10	LOOM
http://purl.bmicc.cn/ontology/ICD10CN/D72.0	International Classification of Diseases, 10th Edition, China	CUI
http://purl.bioontology.org/ontology/MESH/D002609	Medical Subject Headings	CUI