rdfs: label
"autosomal dominant nonsyndromic deafness 13"@en
skos: altLabel
"DEAFNESS, AUTOSOMAL DOMINANT 13"@en
"DEAFNESS, AUTOSOMAL DOMINANT 13; DFNA13"@en
"DFNA13"@en
"Deafness, Autosomal Dominant type 13"@en
"autosomal dominant deafness 13"@en
"autosomal dominant nonsyndromic deafness type 13"@en
schema: description
ar
de
en
uk
"Krankheit"@de
"autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade of life with mid-frequency hearing loss and has material basis in mutation in the COL11A2 gene on chromosome 6p21"@en
"хвороба"@uk
"مرض يصيب الإنسان"@ar
schema: dateModified
"2026-07-05T12:32:55+00:00"^^xsd:dateTime
schema: version
2514121340
wikibase: identifiers
7
wikibase: sitelinks
0
wikibase: statements
15
p: P11430
wd: statement/Q28024672-d22413ac-4195-4c74-e853-bde8e4ad3027
p: P2293
wd: statement/Q28024672-0A1D14F1-19AB-4B76-83C3-415BCB516596
p: P279
wd: statement/Q28024672-0990C5B2-07CE-4B9C-9269-A0E628570843
wd: statement/Q28024672-81932ABA-6EF7-4E31-B716-AA2B97A3844D
p: P2888
wd: statement/Q28024672-130EC4CF-2E43-4048-B65F-5C5962312845
wd: statement/Q28024672-A3772F96-0363-4D5B-94F5-9865A8F78213
p: P2892
wd: statement/Q28024672-1AC3AD33-7699-42B8-B1EF-69503104C440
p: P31
wd: statement/Q28024672-B6684FDF-CEFA-4CAF-ABB3-F59784D96303
wd: statement/Q28024672-D0CBBCC6-8984-4050-B22F-767D1DBE4A20
p: P4229
wd: statement/Q28024672-96F467AD-A93F-48FC-99B4-0B0BC68C035D
p: P486
wd: statement/Q28024672-BD6C9D83-7FA8-43D8-81CB-AFD97031271D
p: P492
wd: statement/Q28024672-6A85F068-059B-48A1-A483-02808E2756A3
p: P5008
wd: statement/Q28024672-55CE1F68-B085-4D45-8DE1-3F915E7176B4
p: P5270
wd: statement/Q28024672-B630E657-A956-4C2A-9873-BDCE7E727BF5
p: P699
wd: statement/Q28024672-5F1074A0-FFF7-4F05-9103-12B32AEEC12A
p: direct-normalized/P486
<http://id.nlm.nih.gov/mesh/C566612>
p: direct-normalized/P5270
<http://purl.obolibrary.org/obo/MONDO_0011159>
p: direct-normalized/P699
<http://purl.obolibrary.org/obo/DOID_DOID:0110545>
wdt: P11430
"DI-00843"
wdt: P2293
COL11A2
wdt: P279
autosomal dominant nonsyndromic deafness
wdt: P2888
<http://identifiers.org/doid/DOID:0110545>
<http://purl.obolibrary.org/obo/DOID_0110545>
wdt: P2892
"C1866095"
wdt: P31
type of disease
rare disease
wdt: P4229
"H90.3"
wdt: P486
"C566612"
wdt: P492
"601868"
wdt: P5008
WikiProject Medicine
wdt: P5270
"MONDO_0011159"
wdt: P699
"DOID:0110545"