SHMARQL

chromosomal disease

<http://www.wikidata.org/entity/Q4501577>

genetic disease that has material basis in extra, missing, or re-arranged chromosomes
rdfs:label
"chromosomal disease"@en
skos:altLabel
"chromosome disorders"@en
"congenital chromosomal disease"@en
schema:description
"genetic disease that has material basis in extra, missing, or re-arranged chromosomes"@en
schema:dateModified "2026-08-07T10:53:04+00:00"^^xsd:dateTime
schema:version 2528400420
wikibase:identifiers 8
wikibase:sitelinks 4
wikibase:statements 19
p:P1995 wd:statement/Q4501577-87B30BD2-7AB7-422F-A03E-E21D6D7BF726
p:P279 wd:statement/Q4501577-C3670155-D1B5-4385-ABCF-29CD27916952
p:P2888 wd:statement/Q4501577-7E02E5D1-94DC-49D7-8020-FA618B990564
wd:statement/Q4501577-CB608C02-EADF-4B67-9C50-79E107417E28
wd:statement/Q4501577-D0DFBCC0-FA5F-4E89-BF79-3359BB6392AA
wd:statement/Q4501577-DF2BA99B-5412-4819-A5C3-79A29CF29B6C
p:P2892 wd:statement/Q4501577-6528B6AF-2974-419D-97E7-A22FD214E5D5
wd:statement/Q4501577-EE48D6B6-B8C4-4E49-B62A-6ACF150DC8BA
p:P2924 wd:statement/Q4501577-4D23DCED-A8E7-45FB-B3FD-6F252E6EC50E
p:P31 wd:statement/Q4501577-C2A5B1A7-0271-4D67-9BFF-A8EAA14749FC
p:P486 wd:statement/Q4501577-2CE2C890-2D83-4AFB-8721-C42B8F8D8352
p:P5008 wd:statement/Q4501577-BC53C649-B20B-4B21-9DF9-9036400922D2
p:P672 wd:statement/Q4501577-40C42751-81CD-4B1D-8CA7-BC679A636EE8
wd:statement/Q4501577-DC5177D4-BE34-4440-BAB6-EC390DE4264C
p:P699 wd:statement/Q4501577-14572233-84A3-4BC9-B03F-72331B9E50F4
wd:statement/Q4501577-F3336D12-67BE-4539-A61B-0B714E0B1422
p:P828 wd:statement/Q4501577-0404A95D-08D6-4789-9317-6250DF441A08
wd:statement/Q4501577-6642793F-BC15-4D9A-BC33-824E5A736AA4
p:P910 wd:statement/Q4501577-1E817D47-8AB5-4885-B1AC-95928979FF00
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D025063>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C16.131.260>
<http://id.nlm.nih.gov/mesh/C16.320.180>
wdt:P1995 medical genetics
wdt:P279 genetic disease
wdt:P2888 <http://identifiers.org/doid/DOID:0080014>
<http://purl.obolibrary.org/obo/DOID_0080014>
wdt:P2892 "C0008626"
"C0969687"
wdt:P2924 "4671415"
wdt:P31 type of disease
wdt:P486 "D025063"
wdt:P5008 WikiProject Medicine
wdt:P672 "C16.131.260"
"C16.320.180"
wdt:P828 pathology
chromosome abnormality
wdt:P910 wd:Q13331409
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