About: Handigodu Syndrome

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

About: Handigodu Syndrome Goto Sponge NotDistinct Permalink

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

medical condition

Attributes	Values
rdf:type	Item
owl:sameAs	Handigodu Syndrome
description	medical condition (en) медичний стан (uk) حالة مرضية (ar)
exact match	wds:Q5647437-2FBA2571-482B-40FC-B481-3E834B4E0264
exact match	http://www.orpha.net/ORDO/Orphanet_99642
Mondo ID	wds:Q5647437-A10C6951-E714-4089-83A5-F382BD6F308F
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0013233
Mondo ID	MONDO_0013233
rdfs:label	ಹಂದಿಗೋಡು ಸಿಂಡ್ರೋಮ್ (kn) Handigodu Syndrome (en) Σύνδρομο Χαντιγκόντου (el) متلازمة هانديجودو (ar) dysplasie spondylo-épimétaphysaire type Handigodu (fr)
skos:prefLabel	ಹಂದಿಗೋಡು ಸಿಂಡ್ರೋಮ್ (kn) Handigodu Syndrome (en) Σύνδρομο Χαντιγκόντου (el) متلازمة هانديجودو (ar) dysplasie spondylo-épimétaphysaire type Handigodu (fr)
name	ಹಂದಿಗೋಡು ಸಿಂಡ್ರೋಮ್ (kn) Handigodu Syndrome (en) Σύνδρομο Χαντιγκόντου (el) متلازمة هانديجودو (ar) dysplasie spondylo-épimétaphysaire type Handigodu (fr)
instance of	wds:Q5647437-188134B3-AFD4-4DED-925A-EC48EF239216 wds:Q5647437-5CEE5EF2-65E8-4903-98DA-488CD75F3A89
instance of	class of disease developmental defect during embryogenesis
subclass of	wds:Q5647437-a451547a-42d3-0bc5-9756-78723e9457fc
subclass of	spondyloepimetaphyseal dysplasia
Orphanet ID	wds:Q5647437-c1b22abf-4adf-1150-74e1-3424f7cc86dd
ICD-10-CM	wds:Q5647437-CAC5B798-DDC2-4890-8F71-E6D5C2C339D4
GARD rare disease ID	wds:Q5647437-8E66724D-7C81-4DAE-896F-46347AD0BE82
OMIM ID	wds:Q5647437-00ed83ee-45c1-f102-0487-927c21abfd67
Orphanet ID	99642
ICD-10-CM	Q77.7
GARD rare disease ID	10741
OMIM ID	613343
skos:altLabel	HANDIGODU JOINT DISEASE (en) Hjd (en) Spondyloepimetaphyseal Dysplasia, Handigodu Type (en)
UMLS CUI	wds:Q5647437-F6D1A759-AF75-43FC-AF8A-B44746B6527B
Microsoft Academic ID	wds:Q5647437-75D3B960-879E-4107-8302-F8499AB9FCF4
ICD-11 (foundation)	wds:Q5647437-7dd965db-4d65-5fcd-cf49-1282b88276f7
Microsoft Academic ID	https://makg.org/entity/2778256927
UMLS CUI	C3150545
Microsoft Academic ID	2778256927
ICD-11 (foundation)	2048058677
is about of	Handigodu Syndrome https://www.wikidata.org/wiki/Special:EntityData/Q5647437 Handigodu syndrome https://ar.wikipedia.org/wiki/%D9%85%D8%AA%D9%84%D8%A7%D8%B2%D9%85%D8%A9_%D9%87%D8%A7%D9%86%D8%AF%D9%8A%D8%AC%D9%88%D8%AF%D9%88 https://el.wikipedia.org/wiki/%CE%A3%CF%8D%CE%BD%CE%B4%CF%81%CE%BF%CE%BC%CE%BF_%CE%A7%CE%B1%CE%BD%CF%84%CE%B9%CE%B3%CE%BA%CF%8C%CE%BD%CF%84%CE%BF%CF%85 https://kn.wikipedia.org/wiki/%E0%B2%B9%E0%B2%82%E0%B2%A6%E0%B2%BF%E0%B2%97%E0%B3%8B%E0%B2%A1%E0%B3%81_%E0%B2%B8%E0%B2%BF%E0%B2%82%E0%B2%A1%E0%B3%8D%E0%B2%B0%E0%B3%8B%E0%B2%AE%E0%B3%8D

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, 196 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software