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230562000: Congenital hypomyelinating neuropathy (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
345474019 Congenital hypomyelinating neuropathy en Synonym Active Entire term case insensitive SNOMED CT core module
345475018 Lyon's hypomyelinating neuropathy en Synonym Active Entire term case sensitive SNOMED CT core module
618389011 Congenital hypomyelinating neuropathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hypomyelinating neuropathy Is a Congenital polyneuropathy false Inferred relationship Existential restriction modifier
Congenital hypomyelinating neuropathy Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital hypomyelinating neuropathy Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier 1
Congenital hypomyelinating neuropathy Finding site Nerve structure false Inferred relationship Existential restriction modifier 2
Congenital hypomyelinating neuropathy Is a Congenital anomaly of the peripheral nervous system false Inferred relationship Existential restriction modifier
Congenital hypomyelinating neuropathy Is a Neuropathy true Inferred relationship Existential restriction modifier
Congenital hypomyelinating neuropathy Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital hypomyelinating neuropathy Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital hypomyelinating neuropathy Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier 1
Congenital hypomyelinating neuropathy Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Congenital hypomyelinating neuropathy Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Congenital hypomyelinating neuropathy Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier 2
Congenital hypomyelinating neuropathy Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital hypomyelinating neuropathy Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 1
Congenital hypomyelinating neuropathy Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital hypomyelinating neuropathy Finding site Nerve structure true Inferred relationship Existential restriction modifier 1
Congenital hypomyelinating neuropathy Associated morphology Hypomyelination true Inferred relationship Existential restriction modifier 1
Congenital hypomyelinating neuropathy Is a Congenital anomaly of nervous system true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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