About: genetic systemic or rheumatologic disease

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: genetic systemic or rheumatologic disease Goto Sponge NotDistinct Permalink

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

instance of systemic or rheumatic disease that is caused by a modification of the individual's genome

Attributes	Values
rdf:type	Item
description	instance of systemic or rheumatic disease that is caused by a modification of the individual's genome (en)
exact match	wds:Q55786852-6A60FD3B-B362-4A54-988C-E6849AEA978E
exact match	http://www.orpha.net/ORDO/Orphanet_271870
Mondo ID	wds:Q55786852-A7048277-142C-46E5-8B52-C3954053E4F2
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0017133
Mondo ID	MONDO_0017133
rdfs:label	genetic systemic or rheumatologic disease (en) genetska sistemska ali revmatološka bolezen (sl)
skos:prefLabel	genetic systemic or rheumatologic disease (en) genetska sistemska ali revmatološka bolezen (sl)
name	genetic systemic or rheumatologic disease (en) genetska sistemska ali revmatološka bolezen (sl)
instance of	wds:Q55786852-9338D0F7-632D-4E75-942E-03A516B46373
instance of	class of disease
subclass of	wds:Q55786852-49E7EE59-33CA-4DDE-BA16-F053B022BE53 wds:Q55786852-FDF868D8-3FC9-4BAE-B885-ED557A2DE2DD
subclass of	genetic disease systemic or rheumatic disease
Orphanet ID	wds:Q55786852-31BE6C03-D78F-4C15-BE82-27A7D99D67F4
Orphanet ID	271870
UMLS CUI	wds:Q55786852-544F98A5-FB59-4214-8320-DCE71C981F34
UMLS CUI	C5680758
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55786852
is subclass of of	cherubism idiopathic juvenile osteoporosis Satoyoshi syndrome camptodactyly-arthropathy-coxa vara-pericarditis syndrome marfanoid intermittent hydrarthrosis Heredofamilial amyloidosis Sneddon syndrome marfanoid–progeroid–lipodystrophy syndrome hereditary pediatric Behçet-like disease PAPA syndrome hereditary periodic fever syndrome sea-blue histiocyte syndrome connective tissue disorder due to lysyl hydroxylase-3 deficiency type 1 interferonopathy retinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome osteonecrosis of genetic origin STAT3-related early-onset multisystem autoimmune disease calciphylaxis cutis mixed autoinflammatory and autoimmune syndrome progeria-associated arthropathy vasculitis, lymphocytic, nodular
is subclass of of	wds:Q684840-1DD5DE03-6E20-48AF-A098-86C458097B65 wds:Q11790313-F79DAC3C-F4EA-4A71-864A-CE02083B6BC9 wds:Q55783900-D11DC721-3EF0-462E-A4F4-986486B6835F wds:Q6318965-6B3F3CB5-CA25-4506-9952-31D065D5E4CD wds:Q55782389-EA8BDD06-0C87-49A7-ACA2-CEBC2F1C18C6 wds:Q55788020-F64525AD-6399-4BCD-AD76-3A72717570A7 wds:Q55788332-9185E4DB-39E4-4472-806B-0DE73F4CF885 wds:Q55786916-8397B932-9164-4ACC-A2F3-54C06C952FBE wds:Q6759035-3BBD24BF-94AA-4409-BD5A-FE59ED454D3B wds:Q5737919-F4780397-DE04-4F88-9DC4-B2EDDB871535 wds:Q55789415-83173F17-B5FE-4950-9052-529D628C33C7 wds:Q30315066-FDDA9AE0-5D83-4A5C-8EBB-7A40303B7397 wds:Q55787617-0CC39AE7-E0F0-4FC3-94D3-012AE43E48AF wds:Q55787621-F7FA5883-0E7A-4657-812B-2D45B2C26437 wds:Q568865-EEA5A8E3-692E-4A39-87EF-47B9634F0A50 wds:Q7426433-EE4BD8DF-5969-4CF7-A29C-93C6CE4D61C9 wds:Q55781600-14F9AC04-5706-4B98-BC8B-A3AE8D58BE05 wds:Q55784815-103F6307-8350-48C3-BE94-15E1E54EF233 wds:Q7118181-4042C29E-3BC6-4F1B-B38C-0142CCFD755C wds:Q5028560-82C063EA-77AD-42ED-83E8-676C37921E8A wds:Q18556319-10745368-1101-4483-95AC-C04FF0771DCE wds:Q55784985-4A322DFB-4844-4288-9284-CCD151273A7E

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 190 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software