About: autosomal recessive severe congenital neutropenia due to CXCR2 deficiency

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About: autosomal recessive severe congenital neutropenia due to CXCR2 deficiency Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

human disease

Attributes	Values
rdf:type	Item
description	human disease (en) хвороба людини (uk)
exact match	wds:Q55788117-332E1BC4-5DE4-447C-98F9-ACA2AAE48498
exact match	http://www.orpha.net/ORDO/Orphanet_420699
Mondo ID	wds:Q55788117-E1330BDA-D015-4B8B-8C97-6ED047BD9224
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0018487
Mondo ID	MONDO_0018487
rdfs:label	autosomal recessive severe congenital neutropenia due to CXCR2 deficiency (en)
skos:prefLabel	autosomal recessive severe congenital neutropenia due to CXCR2 deficiency (en)
name	autosomal recessive severe congenital neutropenia due to CXCR2 deficiency (en)
instance of	wds:Q55788117-310BFC35-ACE9-4048-A975-61512222F703
instance of	class of disease
subclass of	wds:Q55788117-cb4a7b30-4bb4-8f2c-1146-aa6ab802ad9f
subclass of	severe congenital neutropenia
Orphanet ID	wds:Q55788117-6F36D29D-E8B5-490D-9745-0DA237F9A30D
ICD-10-CM	wds:Q55788117-EEBBC8C6-57A3-4D5A-8D44-ABB1E46B39FC
Orphanet ID	420699
ICD-10-CM	D70
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55788117

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