About: PARC syndrome

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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)
exact match	wds:Q55782845-EF91D71A-ADD4-4B42-9B37-3DC646E3D9E0
exact match	http://www.orpha.net/ORDO/Orphanet_2825
Mondo ID	wds:Q55782845-5A7EC969-BA66-42A9-B616-8CBC1FB6D5F3
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0010867
Mondo ID	MONDO_0010867
rdfs:label	PARC syndrome (en) PARC-Syndrom (de) syndrome PARC (fr)
skos:prefLabel	PARC syndrome (en) PARC-Syndrom (de) syndrome PARC (fr)
name	PARC syndrome (en) PARC-Syndrom (de) syndrome PARC (fr)
instance of	wds:Q55782845-6BB72F4A-A526-470D-B4F6-87F9023E2662 wds:Q55782845-704CBFDA-11F4-4D64-B641-B512DD2ADBDC wds:Q55782845-D6F08F66-8212-4FF7-A242-4D6E84815D45
instance of	class of disease head and neck disease developmental defect during embryogenesis
subclass of	wds:Q55782845-7A22303D-0143-4CBF-8BBB-F216EA3FB3A6 wds:Q55782845-828BF71C-324E-4F1A-A7A1-16BE91E25FD0
subclass of	multiple congenital anomalies/dysmorphic syndrome without intellectual disability orofacial clefting syndrome
Orphanet ID	wds:Q55782845-F66C5EB4-D651-4C58-922B-734DADB7EEF0
ICD-10-CM	wds:Q55782845-2C961391-52E8-4E1B-AA7E-95835A922F18
GARD rare disease ID	wds:Q55782845-6B4BCA4D-7BD5-46F5-B7ED-3D9B11B60571
OMIM ID	wds:Q55782845-687EE2CD-8316-4530-8CEF-16A3705150C6
Orphanet ID	2825
ICD-10-CM	Q87.8
GARD rare disease ID	4223
OMIM ID	600331
skos:altLabel	PARC SYNDROME (en) Poikiloderma-alopecia-retrognathism-cleft palate syndrome (en) Poikiloderma, Alopecia, Retrognathism, and Cleft Palate (en)
UMLS CUI	wds:Q55782845-033BB994-64E0-40C0-9E35-1DB71CBCEC67
MeSH descriptor ID	wds:Q55782845-75F7CFD8-9AA2-4ED3-9E75-A03BB5B72963
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/C537174
UMLS CUI	C1838256
MeSH descriptor ID	C537174
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55782845 https://de.wikipedia.org/wiki/PARC-Syndrom

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