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1187643003: Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4675715014 Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4675716010 Autosomal recessive spinocerebellar ataxia type 21 en Synonym Active Entire term case insensitive SNOMED CT core module
4675717018 Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome Is a Spinocerebellar ataxia true Inferred relationship Existential restriction modifier
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome Is a Acute hepatic failure true Inferred relationship Existential restriction modifier
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome Is a Hereditary peripheral neuropathy true Inferred relationship Existential restriction modifier
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome Finding site Peripheral nervous system structure true Inferred relationship Existential restriction modifier 4
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome Occurrence Infancy true Inferred relationship Existential restriction modifier 3
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome Finding site Structure of parenchyma of liver true Inferred relationship Existential restriction modifier 3
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 1
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 2
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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