SHMARQL

autosomal genetic disease

<http://www.wikidata.org/entity/Q18553442>

monogenic disease that is has material basis in a mutation in a single gene on one of the non-sex chromosomes
rdfs:label
"autosomal genetic disease"@en
skos:altLabel
"autosomal hereditary disorder"@en
"autosomal inherited disease"@en
"autosomal inherited disorder"@en
schema:description
"monogenic disease that is has material basis in a mutation in a single gene on one of the non-sex chromosomes"@en
schema:dateModified "2026-09-12T05:45:32+00:00"^^xsd:dateTime
schema:version 2544388254
wikibase:identifiers 2
wikibase:sitelinks 1
wikibase:statements 9
p:P1692 wd:statement/Q18553442-FBFFF77F-A857-4763-95AB-D97A5D8DC255
p:P279 wd:statement/Q18553442-5E34A054-4676-4BF5-B1F1-3B54FF259081
p:P2888 wd:statement/Q18553442-03A5E96D-ACCE-44AF-95BA-7FEC0EB052D4
wd:statement/Q18553442-D24F8DA5-036F-41A6-9071-38A7DD145A51
p:P31 wd:statement/Q18553442-56827363-B92B-4863-ACF5-2870BB797F16
p:P373 wd:statement/Q18553442-2d3b7121-adaf-4a21-85bd-8a3d114c6ba5
p:P5008 wd:statement/Q18553442-CC89EEEF-E3DF-428C-88BC-63B2C6E19EBF
p:P5270 wd:statement/Q18553442-2B4ADA0C-A5BD-4CDE-859B-89E0B5D0B8B4
p:P699 wd:statement/Q18553442-CE05374B-59F1-45A3-9F6C-C7754ED72D1E
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0000429>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0050739>
wdt:P1692 "758.5"
wdt:P279 monogenic disease
wdt:P2888 <http://identifiers.org/doid/DOID:0050739>
<http://purl.obolibrary.org/obo/DOID_0050739>
wdt:P31 type of disease
wdt:P373 "Autosomal diseases"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0000429"
wdt:P699 "DOID:0050739"
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