deafness - CISMeF

Preferred Label : deafness;

MeSH definition : A general term for the complete loss of the ability to hear from both ears.;

DeCS synonym : Deaf Mutism; Bilateral Deafness;

MeSH hyponym : hearing loss, extreme; prelingual deafness; deafness, acquired; Acquired Deafness; Extreme Hearing Loss; Complete Hearing Loss; Deafness, Bilateral; Deafness, Prelingual; Permanent, Deafness; Permanents, Deafness; Hearing Loss Permanent; Permanent, Hearing Loss;

CISMeF hyponym : bilateral deafness; hearing loss, complete;

Related MeSH term : Deaf-Mutism;

MeSH annotation : differentiate from HEARING LOSS, BILATERAL; see various specific terms under HEARING LOSS;

Wikipedia link : https://en.wikipedia.org/wiki/Deafness;

Related CISMeF synonym : deaf mutism;

Details

Origin ID

D003638;

UMLS CUI

C0011053;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- ANGPTL4 wt Allele [NCIt concept]
- Acquired hearing impairment [ICD-11 Category]
- Bilateral Deafness [NCIt concept]
- CD164 molecule [HGNC gene]
- Complete Deafness [NCIt concept]
- Complete deafness (disorder) [SNOMED CT concept]
- Complete hearing loss [MedDRA LLT]
- Deaf [UNESCO concept]
- Deaf [MedDRA LLT]
- Deaf dumbness [UNESCO concept]
- Deaf mutism [PASCAL descriptor]
- Deaf mutism [MedDRA Preferred Term]
- Deaf mutism (disorder) [SNOMED CT concept]
- Deaf mutism, not elsewhere classified [ICD-11 More detail]
- Deafness bilateral [MedDRA Preferred Term]
- Deafness permanent [MedDRA Preferred Term]
- Deafness total [MedDRA LLT]
- LGI1 wt Allele [NCIt concept]
- Other specified forms of hearing loss [ICD-9 code]
- Permanent deafness [MedDRA LLT]
- Prelingual deafness [PASCAL descriptor]
- Prelingual deafness [HPO term]
- Severe hearing impairment [HPO term]
- Severe hearing loss (disorder) [SNOMED CT concept]
- complete deafness [SNOMED Notion]
- deaf mutism, nos [SNOMED Notion]
- hearing disorders and deafness [MedlinePlus Topic]
- hearing problems in children [MedlinePlus Topic]
- solute carrier family 26 member 5 [HGNC gene]
Currated CISMeF NLP mapping
- DEAFNESS [WHO-ART Preferred Term]
- Deafness [MedDRA Preferred Term]
- Deafness [HPMULTI term]
- Deafness [UNESCO concept]
- Deafness [NCIt concept]
- Deafness [HPO term]
- Deafness NOS [MedDRA LLT]
- Deafness disorders [Bloc CIM-11]
- Deafness not otherwise specified [ICD-11 Category]
- Hearing Loss [NCIt concept]
- Hearing impairment [HPO term]
- Hearing loss [PASCAL descriptor]
- Hearing loss [ICD-9 code]
- Hearing loss (disorder) [SNOMED CT concept]
- Hearing loss, unspecified [ICD-10 Sub-category (who)]
- Surdity [MedDRA LLT]
- Unspecified hearing loss [ICD-9 code]
- deafness [Disease (Nov.)]
- deafness [ICPC-2 Rubric]
- deafness, nos [SNOMED Notion]
False automatic mappings
- Bilateral deafness (disorder) [SNOMED CT concept]
HPO term
- Hearing impairment [HPO term]
Indexing information
- COCH protein, human [MeSH Supplementary Concept]
- DIAPH1 protein, human [MeSH Supplementary Concept]
- GSDME protein, human [MeSH Supplementary Concept]
- Gsdme protein, mouse [MeSH Supplementary Concept]
- KPTN protein, human [MeSH Supplementary Concept]
- TBL1X protein, human [MeSH Supplementary Concept]
- TBL1Y protein, human [MeSH Supplementary Concept]
- TMC1 protein, human [MeSH Supplementary Concept]
- TMC2 protein, human [MeSH Supplementary Concept]
- TMC2 protein, mouse [MeSH Supplementary Concept]
- Tbl1x protein, mouse [MeSH Supplementary Concept]
- gsdmeb protein, zebrafish [MeSH Supplementary Concept]
- whrn protein, mouse [MeSH Supplementary Concept]
MedlinePlus topic(s)
- hearing disorders and deafness [MedlinePlus Topic]
Record concept(s)
- Deaf Mutism [MeSH concept]
- Deafness Permanent [MeSH concept]
- Hearing Loss, Complete [MeSH concept]
- deafness [MeSH concept]
- deafness, acquired [MeSH concept]
- hearing loss, extreme [MeSH concept]
- prelingual deafness [MeSH concept]
Related MeSH Supplementary Concept(s)
- Branchiogenic-Deafness syndrome [MeSH Supplementary Concept]
- Burn-Mckeown syndrome [MeSH Supplementary Concept]
- Charcot-Marie-Tooth disease, demyelinating, type 1e [MeSH Supplementary Concept]
- Fine-Lubinsky syndrome [MeSH Supplementary Concept]
- Meyenburg-Altherr-Uehlinger syndrome [MeSH Supplementary Concept]
- Richards-Rundle syndrome [MeSH Supplementary Concept]
- X-linked mental retardation gustavson type [MeSH Supplementary Concept]
- albinism deafness syndrome [MeSH Supplementary Concept]
- arthrogryposis multiplex with deafness, inguinal hernias, and early death [MeSH Supplementary Concept]
- ayazi syndrome [MeSH Supplementary Concept]
- cardioauditory syndrome of sanchez cascos [MeSH Supplementary Concept]
- corneal degeneration, ribbonlike, with deafness [MeSH Supplementary Concept]
- coxoauricular syndrome [MeSH Supplementary Concept]
- davenport donlan syndrome [MeSH Supplementary Concept]
- deafness hyperuricemia neurologic ataxia [MeSH Supplementary Concept]
- deafness, cataract, retinitis pigmentosa, and sperm abnormalities [MeSH Supplementary Concept]
- deafness, congenital onychodystrophy, recessive form [MeSH Supplementary Concept]
- deafness, congenital, and familial myoclonic epilepsy [MeSH Supplementary Concept]
- deafness, congenital, and onychodystrophy, autosomal dominant [MeSH Supplementary Concept]
- deafness, congenital, with vitiligo and achalasia [MeSH Supplementary Concept]
- dementia, familial danish [MeSH Supplementary Concept]
- dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation [MeSH Supplementary Concept]
- emphysema, congenital, with deafness, penoscrotal web, and mental retardation [MeSH Supplementary Concept]
- epiphyseal dysplasia of femoral head, myopia, and deafness [MeSH Supplementary Concept]
- fountain syndrome [MeSH Supplementary Concept]
- herrmann syndrome [MeSH Supplementary Concept]
- hirschsprung disease with polydactyly, renal agenesis, and deafness [MeSH Supplementary Concept]
- hyperlipoproteinemia, type II, and deafness [MeSH Supplementary Concept]
- ichthyosiform erythroderma, corneal involvement, deafness [MeSH Supplementary Concept]
- johnson neuroectodermal syndrome [MeSH Supplementary Concept]
- jones syndrome [MeSH Supplementary Concept]
- keratitis, ichthyosis, and deafness (KID) syndrome [MeSH Supplementary Concept]
- konigsmark knox hussels syndrome [MeSH Supplementary Concept]
- lynch lee murday syndrome [MeSH Supplementary Concept]
- mental retardation-hypotonic facies syndrome, x-linked, 1 [MeSH Supplementary Concept]
- microcephaly deafness syndrome [MeSH Supplementary Concept]
- myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders [MeSH Supplementary Concept]
- myoclonus, cerebellar ataxia, and deafness [MeSH Supplementary Concept]
- nasodigitoacoustic syndrome [MeSH Supplementary Concept]
- nathalie syndrome [MeSH Supplementary Concept]
- nephrosis deafness urinary tract digital malformation [MeSH Supplementary Concept]
- noninsulin-dependent diabetes mellitus with deafness [MeSH Supplementary Concept]
- nonsyndromic deafness [MeSH Supplementary Concept]
- opticocochleodentate degeneration [MeSH Supplementary Concept]
- ramos arroyo clark syndrome [MeSH Supplementary Concept]
- retinitis pigmentosa, X-Linked, and sinorespiratory infections, with or without deafness [MeSH Supplementary Concept]
- schimke X-linked mental retardation syndrome [MeSH Supplementary Concept]
- schlegelberger grote syndrome [MeSH Supplementary Concept]
- secretory diarrhea, myopathy, and deafness [MeSH Supplementary Concept]
- spastic paraplegia 24 [MeSH Supplementary Concept]
- temtamy preaxial brachydactyly syndrome [MeSH Supplementary Concept]
- tibia, absence of, with congenital deafness [MeSH Supplementary Concept]
- tietz syndrome [MeSH Supplementary Concept]
- wells jankovic syndrome [MeSH Supplementary Concept]
- wright dyck syndrome [MeSH Supplementary Concept]
- yemenite deaf-blind hypopigmentation syndrome [MeSH Supplementary Concept]
See also
- Persons with Hearing Disabilities [MeSH Descriptor]
- hearing aids [MeSH Descriptor]
- hearing loss, bilateral [MeSH Descriptor]
- lipreading [MeSH Descriptor]
See also (suggested by CISMeF)
- Education of Persons with Hearing Disabilities [MeSH Descriptor]
- nephritis, hereditary [MeSH Descriptor]
- sign language [MeSH Descriptor]
Semantic type(s)
- Finding [UMLS semantic type]
UMLS correspondences (same concept)
- Cophosis [MedDRA LLT]
- DEAFNESS [WHO-ART Preferred Term]
- Deafness [MedDRA Preferred Term]
- Deafness [HPO term]
- Deafness [NCIt concept]
- Deafness NOS [MedDRA LLT]
- No hearing [MedDRA LLT]
- Surdity [MedDRA LLT]
- Unspecified deafness [MedDRA LLT]
- deafness [ICPC-2 Rubric]
- deafness [Disease (Nov.)]
- deafness, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- Deaf mutism (disorder) [SNOMED CT concept]
- acquired deafness [Disease (Nov.)]
- bilateral deafness [Disease (Nov.)]
- prelingual deafness [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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