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782690007: Gemignani syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3755229018 Spinocerebellar ataxia, amyotrophy, deafness syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3755230011 Gemignani syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3755231010 Gemignani syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3755232015 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3755233013 A rare neurodegenerative disease characterised by slowly progressive ataxia, amyotrophy of the hands and distal arms, spastic paraplegia, progressive sensorineural hearing loss, hypogonadism and short stature. Additional features include generalised cerebellar atrophy and peripheral nervous system anomalies. Small cervical spinal cord, intellectual/language disability and localised vitiligo have also been reported. There have been no further descriptions in the literature since 1989. 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
Gemignani syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Gemignani syndrome (disorder) Is a Hearing loss associated with syndrome true Inferred relationship Some
Gemignani syndrome (disorder) Is a Chronic disease of ear false Inferred relationship Some
Gemignani syndrome (disorder) Finding site Structure of central nervous system (body structure) true Inferred relationship Some 1
Gemignani syndrome (disorder) Is a Cerebellar ataxia true Inferred relationship Some
Gemignani syndrome (disorder) Is a Hereditary disorder of nervous system false Inferred relationship Some
Gemignani syndrome (disorder) Is a Chronic brain syndrome true Inferred relationship Some
Gemignani syndrome (disorder) Is a Hereditary ataxia (disorder) true Inferred relationship Some
Gemignani syndrome (disorder) Is a Auditory system hereditary disorder true Inferred relationship Some
Gemignani syndrome (disorder) Is a Degenerative disease of the central nervous system false Inferred relationship Some
Gemignani syndrome (disorder) Associated morphology dégénérescence false Inferred relationship Some 1
Gemignani syndrome (disorder) Is a Sensorineural hearing loss true Inferred relationship Some
Gemignani syndrome (disorder) Finding site Ear structure true Inferred relationship Some 4
Gemignani syndrome (disorder) Finding site Cerebellar structure true Inferred relationship Some 3
Gemignani syndrome (disorder) Interprets Hearing true Inferred relationship Some 5
Gemignani syndrome (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 2
Gemignani syndrome (disorder) Is a Hereditary degenerative disease of central nervous system true Inferred relationship Some
Gemignani syndrome (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 1
Gemignani syndrome (disorder) Is a Chronic deafness true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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