About: Witkop-Von Sallmann disease

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About: Witkop-Von Sallmann disease 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) مرض يصيب الإنسان (ar) 病症 (zh)
exact match	wds:Q18975153-05DD2345-3969-48F4-AB1E-8160DBBDFA6C wds:Q18975153-56F294FC-2D60-416A-8D9D-D4777DD1D9D4 wds:Q18975153-FC569974-C660-4174-AD69-5D9B2D3CE7A2
exact match	http://www.orpha.net/ORDO/Orphanet_352657
Mondo ID	wds:Q18975153-A52133B4-7229-494A-B0AE-4039B73A64A1
Disease Ontology ID	wds:Q18975153-326C58FA-5385-4B33-ACD2-D7703B276596
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0007486
Mondo ID	MONDO_0007486
rdfs:label	Witkop-Von Sallmann disease (en) 遗传性良性上皮内角化不良综合征 (zh) dyskératose intraépithéliale héréditaire bénigne (fr)
skos:prefLabel	Witkop-Von Sallmann disease (en) 遗传性良性上皮内角化不良综合征 (zh) dyskératose intraépithéliale héréditaire bénigne (fr)
name	Witkop-Von Sallmann disease (en) 遗传性良性上皮内角化不良综合征 (zh) dyskératose intraépithéliale héréditaire bénigne (fr)
instance of	wds:Q18975153-38E07006-EC9C-46A7-8B1F-456E2ECC8599
instance of	class of disease
subclass of	wds:Q18975153-59FFC6D3-8B32-4A24-88BE-1836C00BFD4C wds:Q18975153-89B829E0-4AA7-4C5F-A5A4-BEF0CC9ECF75
subclass of	syndromic corneal dystrophy epithelial and subepithelial dystrophy
Google Knowledge Graph ID	wds:Q18975153-89E8290F-9A98-4276-8C16-FB04759C84E8
Google Knowledge Graph ID	http://g.co/kg/g/11bwd_sp25
Google Knowledge Graph ID	/g/11bwd_sp25
Orphanet ID	wds:Q18975153-5c7a4c66-4394-2f71-0394-b3c8d1377386
ICD-10-CM	wds:Q18975153-593FD252-E28C-4BF2-BDBD-3118805A002E
Orphanet ID	352657
ICD-10-CM	Q82.8
skos:altLabel	Hereditary benign intraepithelial dyskeratosis (en) HBID (en) Hereditary benign corneal intraepithelial dyskeratosis (en) DYSKERATOSIS, HEREDITARY BENIGN INTRAEPITHELIAL (en) Dkbi (en) Witkop-Von Sallmann Disease (en) obsolete Witkop-Von Sallmann disease (en) DYSKERATOSIS, HEREDITARY BENIGN INTRAEPITHELIAL; HBID (en) Hereditary benign intraepithelial dyskeratosis (disorder) (en)
UMLS CUI	wds:Q18975153-fcfb121d-4f76-8364-29f7-0ec70a547916
MeSH descriptor ID	wds:Q18975153-2860DB1A-02D6-40E3-B824-7E74B0FA890A
on focus list of Wikimedia project	wds:Q18975153-85B6B215-3A5F-4E75-B0E6-B755D4506B7A
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/C562551
UMLS CUI	C0265966
MeSH descriptor ID	C562551
on focus list of Wikimedia project	WikiProject Medicine
is owl:sameAs of	Witkop-Von Sallmann disease
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q18975153 Hereditary benign intraepithelial dyskeratosis

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