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1003447007: Pelizaeus-Merzbacher disease null syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4164742011 PLP1 null syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
4168274013 Null syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4283397018 Pelizaeus-Merzbacher disease null syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
4283398011 Pelizaeus-Merzbacher disease null syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pelizaeus-Merzbacher disease null syndrome Is a Congenital degeneration of nervous system true Inferred relationship Existential restriction modifier
Pelizaeus-Merzbacher disease null syndrome Is a Congenital anomaly of central nervous system true Inferred relationship Existential restriction modifier
Pelizaeus-Merzbacher disease null syndrome Finding site Myelinated nerve fiber structure true Inferred relationship Existential restriction modifier 1
Pelizaeus-Merzbacher disease null syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Pelizaeus-Merzbacher disease null syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Pelizaeus-Merzbacher disease null syndrome Associated morphology Myelin sheath alteration true Inferred relationship Existential restriction modifier 1
Pelizaeus-Merzbacher disease null syndrome Finding site White matter structure of brain and spinal cord true Inferred relationship Existential restriction modifier 2
Pelizaeus-Merzbacher disease null syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Pelizaeus-Merzbacher disease null syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 2
Pelizaeus-Merzbacher disease null syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Pelizaeus-Merzbacher disease null syndrome Is a Pelizaeus-Merzbacher disease true Inferred relationship Existential restriction modifier
Pelizaeus-Merzbacher disease null syndrome Is a X-linked recessive hereditary disease 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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