|
rdfs:label
|
"autosomal dominant nonsyndromic deafness 69"@en
|
|
skos:altLabel
|
"DCUA"@en
|
|
"DFNA69"@en
|
|
"Deafness, Congenital, Unilateral or Asymmetric"@en
|
|
"autosomal dominant deafness 69"@en
|
|
"autosomal dominant nonsyndromic deafness type 69"@en
|
|
"unilateral or asymmetric congenital deafness"@en
|
|
schema:description
|
"Krankheit"@de
"autosomal dominant nonsyndromic deafness that has material basis in mutation in the KITLG gene on chromosome 12q21"@en
"хвороба"@uk
"مرض يصيب الإنسان"@ar
|
|
schema:dateModified
|
"2026-07-05T12:33:11+00:00"^^xsd:dateTime
|
|
schema:version
|
2514121422
|
|
wikibase:identifiers
|
6
|
|
wikibase:sitelinks
|
0
|
|
wikibase:statements
|
14
|
|
p:P11430
|
wd:statement/Q28024720-8cb34520-491b-e63b-3270-527b4fa7f6f3
|
|
p:P2293
|
wd:statement/Q28024720-1AAD7C2B-CE9B-42B0-8157-97790F5BE02B
|
|
p:P279
|
wd:statement/Q28024720-148252D5-33E6-43D8-8E48-E22B0A411548
|
|
wd:statement/Q28024720-A4CCE6C9-A9D0-49A6-99EE-C2470CB3E13C
|
|
p:P2888
|
wd:statement/Q28024720-E02243B9-6275-4B18-A143-04CA89EB036A
|
|
wd:statement/Q28024720-FB42E86E-1EC7-4C14-B54B-F628A2C11209
|
|
p:P2892
|
wd:statement/Q28024720-F2547ACB-FA23-4367-9A71-4CF8A1BD5081
|
|
p:P31
|
wd:statement/Q28024720-343A27CA-6A74-4A0A-B274-954A176000A4
|
|
wd:statement/Q28024720-B7504117-D32E-4640-89D7-7D250E9A21C7
|
|
p:P4229
|
wd:statement/Q28024720-9ED2BB8A-10CC-40AE-B03D-588BFD4CB2B7
|
|
p:P492
|
wd:statement/Q28024720-CCDFEC2E-C4BB-4C2B-B99E-792801786AB1
|
|
p:P5008
|
wd:statement/Q28024720-3202A1C3-0C0A-4BEE-8280-37CC7FA45308
|
|
p:P5270
|
wd:statement/Q28024720-7944898E-7B2D-4306-9EC5-551647E4AF7C
|
|
p:P699
|
wd:statement/Q28024720-B6489BB4-CC33-486D-A1DC-F5CF9756F190
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0014738>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:0110590>
|
|
wdt:P11430
|
"DI-04598"
|
|
wdt:P2293
|
KITLG
|
|
wdt:P279
|
autosomal dominant nonsyndromic deafness
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:0110590>
|
|
<http://purl.obolibrary.org/obo/DOID_0110590>
|
|
wdt:P2892
|
"C4225241"
|
|
wdt:P31
|
type of disease
|
|
rare disease
|
|
wdt:P4229
|
"H90.3"
|
|
wdt:P492
|
"616697"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0014738"
|
|
wdt:P699
|
"DOID:0110590"
|