FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

723452007: Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3424676019 Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424677011 Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424678018 PHARC (polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3424679014 PHARC syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3424680012 Peripheral neuropathy Fiskerstrand type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5403074016 This rare neurologic disease is a slowly progressive Refsum-like disorder associating signs of peripheral neuropathy with late-onset hearing loss, cataract and pigmentary retinopathy that become evident during the third decade of life. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder) Is a Polyneuropathy true Inferred relationship Some
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder) Is a Autosomal recessive retinitis pigmentosa true Inferred relationship Some
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder) Is a Hearing loss associated with syndrome true Inferred relationship Some
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder) Is a Disorder of lipid metabolism true Inferred relationship Some
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder) Is a Auditory system hereditary disorder true Inferred relationship Some
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder) Is a Hereditary disorder of nervous system true Inferred relationship Some
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder) Finding site Peripheral nerve structure true Inferred relationship Some 2
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder) Finding site Ear structure false Inferred relationship Some 1
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder) Associated morphology Dystrophy true Inferred relationship Some 3
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder) Finding site Retinal structure true Inferred relationship Some 3
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder) Finding site Structure of auditory system (body structure) true Inferred relationship Some 1
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder) Interprets Hearing true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start