rdfs: label
ar
bs
ca
en
es
fr
it
pt
pt-br
sl
zh
zh-cn
zh-hans
zh-hant
"Nesindromska gluhoća"@bs
"Sordera no sindrómica"@es
"nesindromska gluhost"@sl
"nonsyndromic deafness"@en
"sordesa no sindromica"@ca
"sordità non sindromica"@it
"surdez hereditária não-sindrômica"@pt
"surdez hereditária não-sindrômica"@pt-br
"surdité génétique non syndromique"@fr
"الصمم غير المتلازمي"@ar
"非症候群型听觉障碍"@zh-hans
"非症候群型聽覺障礙"@zh-hant
"非綜合徵型耳聾"@zh
"非综合征性耳聋"@zh-cn
skos: altLabel
en
es
fr
zh
"Familial deafness"@en
"Isolated genetic deafness"@en
"Non-syndromic genetic deafness"@en
"Sordera no sindromica"@es
"Surdité génétique isolée"@fr
"nonsyndromic hearing loss"@en
"nonsyndromic hereditary hearing loss"@en
"非症候群型听觉障碍"@zh
"非綜合徵型耳聾 (常染色體顯性遺傳)"@zh
schema: description
ca
de
en
it
sl
uk
"Krankheit"@de
"auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms"@en
"genetsko pogojena okvara slušnega sistema, ki je povezana s trajno izgubo sluha zaradi poškodbe struktur v notranjem in/ali srednjem ušesu in je ne spremljajo drugi znaki ali simptomi"@sl
"malaltia del sistema auditiu associada a una pèrdua auditiva permanent causada per danys a les estructures de l'oïda interna i/o de l'oïda mitjana, que no s'associa amb altres signes i símptomes."@ca
"malattia"@it
"хвороба"@uk
schema: dateModified
"2026-10-24T00:40:20+00:00"^^xsd:dateTime
schema: version
2560167849
wikibase: identifiers
12
wikibase: sitelinks
5
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114
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<http://id.nlm.nih.gov/mesh/C580334>
p: direct-normalized/P5270
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<https://makg.org/entity/2779163945>
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<http://purl.obolibrary.org/obo/DOID_DOID:0050563>
wdt: P11143
"Nonsyndromic deafness"
wdt: P11956
"0009076"
wdt: P14914
"D87884"
wdt: P1550
"87884"
wdt: P2293
DCDC2
SLC26A4
CD164
MYO7A
ACTG1
COL11A2
CRYM
COCH
EYA4
FOXI1
GJB3
TNC
KCNJ10
MAP1B
MYH9
MYO1A
MYO6
ROR1
PDE1C
POU3F4
POU4F3
PRPS1
RDX
TECTA
WFS1
TRRAP
CLDN9
AIFM1
KCNQ4
S1PR2
OTOF
RIPOR2
USH1C
CIB2
GJB6
TRIOBP
PPIP5K2
DMXL2
CLDN14
SMPX
WHRN
GPSM2
MYO15A
CABP2
MYO3A
BDP1
TBC1D24
CDH23
TMPRSS3
EPS8L2
PCDH15
SPATA5L1
MYH14
PDZD7
GRHL2
GREB1L
DIAPH3
ESPN
USP48
PNPT1
PKHD1L1
TMC1
USH1G
TMEM132E
LOXHD1
GIPC3
OTOA
CCDC50
MARVELD2
STRC
SYNE4
LRTOMT
LHFPL5
MSRB3
TMIE
OTOGL
TPRN
ILDR1
OTOG
PTPRQ
CEACAM16
GRXCR1
CENPP
MIR96
PJVK
CLRN2
MINAR2
REST
COL11A1
ESRRB
wdt: P279
genetic deafness
rare deafness
wdt: P2841
neonatal onset
infantile onset
wdt: P2888
<http://identifiers.org/doid/DOID:0050563>
<http://purl.obolibrary.org/obo/DOID_0050563>
<http://www.orpha.net/ORDO/Orphanet_87884>
wdt: P2892
"C5680182"
wdt: P31
type of disease
wdt: P4229
"H90.5"
wdt: P4317
"6410"
wdt: P486
"C580334"
wdt: P494
"H90.5"
wdt: P5008
WikiProject Hearing Health
WikiProject Medicine
wdt: P5270
"MONDO_0019497"
wdt: P6366
"2779163945"
wdt: P699
"DOID:0050563"