About: Ramon syndrome

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About: Ramon syndrome 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) մարդու հիվանդություն (hy) хвороба людини (uk) seltene Erkrankung (de)
exact match	wds:Q18027110-01248FAD-FAEB-41CA-8FF1-4373244D4851
exact match	http://www.orpha.net/ORDO/Orphanet_3019
Mondo ID	wds:Q18027110-EEE1F644-521D-45C9-8217-AA707DB7C528
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0009954
Mondo ID	MONDO_0009954
rdfs:label	Ramon sendromu (tr) Ramon syndrome (en) Ramon-Syndrom (de) syndrome de Ramon (fr)
skos:prefLabel	Ramon sendromu (tr) Ramon syndrome (en) Ramon-Syndrom (de) syndrome de Ramon (fr)
name	Ramon sendromu (tr) Ramon syndrome (en) Ramon-Syndrom (de) syndrome de Ramon (fr)
instance of	wds:Q18027110-4D173B68-E9F7-409F-9570-19CB41769282 wds:Q18027110-986801B4-0F5E-455F-B975-369F6504EB56 wds:Q18027110-BB0547F0-81D7-4BE3-81FE-CC11AE2CE16D
instance of	class of disease hereditary disorder developmental defect during embryogenesis
subclass of	wds:Q18027110-4B0397B4-7398-46D4-8671-90BF25163CD3 wds:Q18027110-BA6FBE54-1E21-4F91-BC2C-B8C62B6F4229 wds:Q18027110-b5c9aaa8-43db-974d-ad32-b8dd714957f9
subclass of	cherubism malformation syndrome with odontal and/or periodontal component primary bone dysplasia with disorganized development of skeletal components
Orphanet ID	wds:Q18027110-81283149-47b0-8586-fef3-beba57cb765d
ICD-10-CM	wds:Q18027110-60B01C62-1FEA-463E-8583-57AF930B918C
GARD rare disease ID	wds:Q18027110-E226DFBE-7A43-4C9C-8C5B-3540B9645194
OMIM ID	wds:Q18027110-0d5eeae5-4410-4dc3-fb70-52e7fe470507
Orphanet ID	3019
ICD-10-CM	Q87.8
GARD rare disease ID	7523
OMIM ID	266270
skos:altLabel	Gingival fibromatosis combined with cherubism (en) RAMON SYNDROME (en) Cherubism, Gingival Fibromatosis, Epilepsy, Mental Deficiency, Hypertrichosis, and Stunted Growth (en) Cherubism-gingival fibromatosis-intellectual disability syndrome (en)
UMLS CUI	wds:Q18027110-C4CB77B2-52AC-4992-9DA2-F46E1B912A66
MeSH descriptor ID	wds:Q18027110-38b7c161-4290-d490-32bd-738fb5c0a08e
ICD-11 (foundation)	wds:Q18027110-51E8926C-E186-480C-B040-05211E120B57
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/C535285
UMLS CUI	C0796133
MeSH descriptor ID	C535285
ICD-11 (foundation)	122538435
is owl:sameAs of	Ramon syndrome
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q18027110 https://de.wikipedia.org/wiki/Ramon-Syndrom https://tr.wikipedia.org/wiki/Ramon_sendromu
is main subject of	Cherubism, gingival fibromatosis, epilepsy, and mental deficiency (Ramon syndrome) with juvenile rheumatoid arthritis. Retinal changes and tumorigenesis in Ramon syndrome: follow-up of a Brazilian family Cherubism combined with epilepsy, mental retardation and gingival fibromatosis (Ramon syndrome): a case report Axenfeld anomaly and retinal changes in Ramon syndrome: follow-up of two sibs Ramon syndrome with diabetes mellitus and vascular skin lesions in two sibs
is main subject of	wds:Q74476746-129DBF1E-B11A-4DD2-9DEC-2C72C5E95624 wds:Q43825020-7D11B001-53B3-4A79-A9FA-4D12D4A79FD8 wds:Q33885564-BCB868D0-8EEF-44AD-A444-61AC5FA6F77A wds:Q35244899-96941344-CD6E-485E-A76C-787EE6132877 wds:Q52077266-D77E0EF9-B344-455D-9084-6101A28AB087

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