rdfs: label
"autosomal dominant nonsyndromic deafness 9"@en
skos: altLabel
"DEAFNESS, AUTOSOMAL DOMINANT 9"@en
"DEAFNESS, AUTOSOMAL DOMINANT 9; DFNA9"@en
"DFNA9"@en
"Deafness, Autosomal Dominant type 9"@en
"autosomal dominant deafness 9"@en
"autosomal dominant nonsyndromic deafness type 9"@en
schema: description
ar
de
en
uk
"Krankheit"@de
"autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade with high frequency progressive hearing loss and has material basis in mutation in the COCH gene on chromosome 14q12"@en
"хвороба"@uk
"مرض يصيب الإنسان"@ar
schema: dateModified
"2026-07-05T12:33:12+00:00"^^xsd:dateTime
schema: version
2514121428
wikibase: identifiers
7
wikibase: sitelinks
0
wikibase: statements
15
p: P11430
wd: statement/Q28024723-d1d4f4ce-4c29-3a13-4993-2d79d02f02c1
p: P2293
wd: statement/Q28024723-8E02F765-AA70-43E9-83F6-CD2C34043034
p: P279
wd: statement/Q28024723-0F453215-1337-4B33-A012-78988B292E92
wd: statement/Q28024723-804E7A12-45C6-4958-BCF2-6E6D07F6E9DF
p: P2888
wd: statement/Q28024723-5A3D7905-5711-4074-9E2E-B150ED4EF0F7
wd: statement/Q28024723-9FC06326-B720-4A56-A747-274E2784878D
p: P2892
wd: statement/Q28024723-E457093E-205E-4341-84F4-F365344B4B7E
p: P31
wd: statement/Q28024723-095D0CA2-9A63-4E10-8DC6-503FA9D67EF3
wd: statement/Q28024723-7871A59B-E807-4033-A8DF-7E83B5D6DE7C
p: P4229
wd: statement/Q28024723-BAD1C0D8-95E5-4EF0-9054-4577A91B4FD7
p: P486
wd: statement/Q28024723-216FEC43-AB20-49F4-815C-F718F2DCC71A
p: P492
wd: statement/Q28024723-629E8D2F-4122-4F53-A9F7-57711436430E
p: P5008
wd: statement/Q28024723-F15E6BC7-6B3D-4768-BD5F-8540DD2BA27D
p: P5270
wd: statement/Q28024723-F0B7DF75-4BC3-4C2F-8E3D-99E569036011
p: P699
wd: statement/Q28024723-3D5FA8F3-5688-4AB2-AA50-A8E92E2DA9E4
p: direct-normalized/P486
<http://id.nlm.nih.gov/mesh/C563335>
p: direct-normalized/P5270
<http://purl.obolibrary.org/obo/MONDO_0011058>
p: direct-normalized/P699
<http://purl.obolibrary.org/obo/DOID_DOID:0110593>
wdt: P11430
"DI-00839"
wdt: P2293
COCH
wdt: P279
autosomal dominant nonsyndromic deafness
wdt: P2888
<http://identifiers.org/doid/DOID:0110593>
<http://purl.obolibrary.org/obo/DOID_0110593>
wdt: P2892
"C1832425"
wdt: P31
type of disease
rare disease
wdt: P4229
"H90.3"
wdt: P486
"C563335"
wdt: P492
"601369"
wdt: P5008
WikiProject Medicine
wdt: P5270
"MONDO_0011058"
wdt: P699
"DOID:0110593"