About: acryocystitis-osteopoikilosis syndrome

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About: acryocystitis-osteopoikilosis syndrome Goto Sponge NotDistinct Permalink

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

Attributes	Values
rdf:type	Item
ICD-10	wds:Q29014964-36b6c2fd-4a04-b2ec-9411-4050971f40c7 wds:Q29014964-ccb0d658-48e1-5392-463f-91f684d86b08
Mondo ID	wds:Q29014964-5D3D1862-319B-42D7-8049-D1535317E57B
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0008158
ICD-10	Q78.8 H04.3
Mondo ID	MONDO_0008158
rdfs:label	Günal-Seber-Başaran-Syndrom (de) acryocystitis-osteopoikilosis syndrome (en) syndrome de dacryocystite-ostéopoecilie (fr)
skos:prefLabel	Günal-Seber-Başaran-Syndrom (de) acryocystitis-osteopoikilosis syndrome (en) syndrome de dacryocystite-ostéopoecilie (fr)
name	Günal-Seber-Başaran-Syndrom (de) acryocystitis-osteopoikilosis syndrome (en) syndrome de dacryocystite-ostéopoecilie (fr)
instance of	wds:Q29014964-24622C67-9D55-4F39-8383-D4BF05B1F875 wds:Q29014964-34C198C4-980F-424B-B4EA-758BB85C2875 wds:Q29014964-8CB2B4C1-E9C0-4C24-A0F7-1DA52C05189C
instance of	class of disease genetic disease developmental defect during embryogenesis
subclass of	wds:Q29014964-44054ac2-4332-bfd5-ed35-f30453db5ecf wds:Q29014964-783d32e3-42de-c339-3808-4b8989129bc8 wds:Q29014964-E1198670-2CF8-4E7C-9D39-9B9B17042CA2
subclass of	dacryocystitis primary bone dysplasia with increased bone density osteopoikilosis
Orphanet ID	wds:Q29014964-6d662797-4801-ca1d-a720-e7b5dc10a51f
OMIM ID	wds:Q29014964-b2b5761c-497b-c831-b166-860d6ef7a0f3
Orphanet ID	1562
OMIM ID	166705
Medical Dictionary...ory Activities ID	wds:Q29014964-5147EB14-E2EA-4452-A7F6-6C39BD142D0D
Medical Dictionary...ory Activities ID	http://purl.bioontology.org/ontology/MDRFRE/10087151
Medical Dictionary...ory Activities ID	10087151
skos:altLabel	Gunal-Seber-Basaran syndrome (en) OSTEOPOIKILOSIS AND DACRYOCYSTITIS (en) Syndrome de Gunal-Seber-Basaran (fr)
UMLS CUI	wds:Q29014964-35eadf1c-4ed7-0b80-3e6c-691c3dfeda1a
MeSH descriptor ID	wds:Q29014964-bc8d9794-45c1-a48d-811a-da1c910349b2
ICD-11 (foundation)	wds:Q29014964-1AC802BF-9793-46E3-9C98-C3CE4D3E2B65
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/C536061
UMLS CUI	C1833698
MeSH descriptor ID	C536061
ICD-11 (foundation)	1520254601
mode of inheritance	wds:Q29014964-E3D2E72D-55B2-4A75-8AE3-08774CF5D278
mode of inheritance	autosomal dominant
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q29014964 https://de.wikipedia.org/wiki/G%C3%BCnal-Seber-Ba%C5%9Faran-Syndrom

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