|
rdfs:label
|
"autosomal recessive nonsyndromic deafness 84B"@en
|
|
skos:altLabel
|
"DEAFNESS, AUTOSOMAL RECESSIVE 84B"@en
|
|
"DEAFNESS, AUTOSOMAL RECESSIVE 84B; DFNB84B"@en
|
|
"DFNB84B"@en
|
|
"Deafness, Autosomal Recessive type 84B"@en
|
|
"autosomal recessive deafness 84B"@en
|
|
"autosomal recessive nonsyndromic deafness type 84B"@en
|
|
schema:description
|
"Krankheit"@de
"autosomal recessive nonsyndromic deafness that has material basis in mutation in the OTOGL gene on chromosome 12q21"@en
"хвороба"@uk
"مرض يصيب الإنسان"@ar
|
|
schema:dateModified
|
"2026-07-05T12:34:03+00:00"^^xsd:dateTime
|
|
schema:version
|
2514121700
|
|
wikibase:identifiers
|
6
|
|
wikibase:sitelinks
|
0
|
|
wikibase:statements
|
14
|
|
p:P11430
|
wd:statement/Q28024657-263098a7-4b96-a497-9087-8186213a70ee
|
|
p:P2293
|
wd:statement/Q28024657-BE9092EB-C398-4054-A3B3-CF59444752FE
|
|
p:P279
|
wd:statement/Q28024657-6BCC15B1-C0EB-4BC8-9DAF-22418F9FA897
|
|
wd:statement/Q28024657-CD2758A7-D896-4CD9-B278-649ED22AEBD3
|
|
p:P2888
|
wd:statement/Q28024657-C8A392C0-291F-4C52-B8DB-75A5240D9A8B
|
|
wd:statement/Q28024657-E7A6A44F-F3D4-492E-A0E7-832268C7ED06
|
|
p:P2892
|
wd:statement/Q28024657-C59B2315-7177-46C8-AE5E-47C652B87C98
|
|
p:P31
|
wd:statement/Q28024657-31599AA7-E063-415B-B08F-74E41BF05307
|
|
wd:statement/Q28024657-FE331D46-F29E-43B2-A124-380F4DDC94F9
|
|
p:P4229
|
wd:statement/Q28024657-9EF95DFD-2817-4F42-943F-4530BE37B8A7
|
|
p:P492
|
wd:statement/Q28024657-80EE0DBB-A9BD-487E-824C-4003352F72E8
|
|
p:P5008
|
wd:statement/Q28024657-25BEF3F6-58B6-40FA-8654-3B34F611841B
|
|
p:P5270
|
wd:statement/Q28024657-F2788269-4547-4B26-86C8-D33E671CD02C
|
|
p:P699
|
wd:statement/Q28024657-7CDFA57E-23F0-40E3-9342-EC7AD1CD2FF5
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0013984>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:0110530>
|
|
wdt:P11430
|
"DI-03565"
|
|
wdt:P2293
|
OTOGL
|
|
wdt:P279
|
autosomal recessive nonsyndromic deafness
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:0110530>
|
|
<http://purl.obolibrary.org/obo/DOID_0110530>
|
|
wdt:P2892
|
"C3554159"
|
|
wdt:P31
|
type of disease
|
|
rare disease
|
|
wdt:P4229
|
"H90.3"
|
|
wdt:P492
|
"614944"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0013984"
|
|
wdt:P699
|
"DOID:0110530"
|