FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

232325008: Chronic deafness (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Oct 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
348075014 Chronic deafness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2570126019 Chronic deafness (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
348075014 Chronic deafness en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
348075014 Chronic deafness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
620375018 Chronic deafness (finding) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2570126019 Chronic deafness (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2570126019 Chronic deafness (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
307811000077113 surdité chronique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
307811000077113 surdité chronique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chronic deafness Is a Hearing loss true Inferred relationship Existential restriction modifier (core metadata concept)
Chronic deafness Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Chronic deafness Finding site Ear structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Chronic deafness Interprets Hearing false Inferred relationship Existential restriction modifier (core metadata concept)
Chronic deafness Interprets Ability to hear (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept)
Chronic deafness Interprets entité observable fonctionnelle false Inferred relationship Existential restriction modifier (core metadata concept)
Chronic deafness Is a Disorder of ear false Inferred relationship Existential restriction modifier (core metadata concept)
Chronic deafness Interprets Hearing true Inferred relationship Existential restriction modifier (core metadata concept) 2
Chronic deafness Is a Chronic disease of ear (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Chronic deafness Clinical course Chronic (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Is a True Chronic deafness Inferred relationship Existential restriction modifier (core metadata concept)
Multiple epiphyseal dysplasia Beighton type (disorder) Is a True Chronic deafness Inferred relationship Existential restriction modifier (core metadata concept)
A rare multiple congenital anomalies syndrome characterized by cutaneous mastocytosis, microcephaly, microtia and/or hearing loss, hypotonia and skeletal anomalies (e.g. clinodactyly, camptodactyly, scoliosis). Additional common features are short stature, intellectual disability and difficulties. Facial dysmorphism may include upslanted palpebral fissures, highly arched palate and micrognathia. Rarely, seizures and asymmetrically small feet have been reported. Is a True Chronic deafness Inferred relationship Existential restriction modifier (core metadata concept)
Spastic paraplegia, nephritis, deafness syndrome Is a True Chronic deafness Inferred relationship Existential restriction modifier (core metadata concept)
A rare neurodegenerative disease characterized by slowly progressive ataxia, amyotrophy of the hands and distal arms, spastic paraplegia, progressive sensorineural hearing loss, hypogonadism and short stature. Additional features include generalized cerebellar atrophy and peripheral nervous system anomalies. Small cervical spinal cord, intellectual/language disability and localized vitiligo have also been reported. There have been no further descriptions in the literature since 1989. Is a True Chronic deafness Inferred relationship Existential restriction modifier (core metadata concept)
Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome Is a True Chronic deafness Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start