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1003881009: Pelizaeus-Merzbacher disease in female carrier (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
4166883019 Pelizaeus-Merzbacher disease in female carrier en Synonym Active Entire term case sensitive SNOMED CT core module
4166884013 Pelizaeus-Merzbacher disease in female carrier (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 in female carrier Is a Pelizaeus-Merzbacher disease true Inferred relationship Existential restriction modifier
Pelizaeus-Merzbacher disease in female carrier Is a Congenital degeneration of nervous system true Inferred relationship Existential restriction modifier
Pelizaeus-Merzbacher disease in female carrier Is a Congenital anomaly of central nervous system true Inferred relationship Existential restriction modifier
Pelizaeus-Merzbacher disease in female carrier Finding site Myelinated nerve fiber structure true Inferred relationship Existential restriction modifier 1
Pelizaeus-Merzbacher disease in female carrier Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Pelizaeus-Merzbacher disease in female carrier Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Pelizaeus-Merzbacher disease in female carrier Associated morphology Myelin sheath alteration true Inferred relationship Existential restriction modifier 1
Pelizaeus-Merzbacher disease in female carrier Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 2
Pelizaeus-Merzbacher disease in female carrier Finding site White matter structure of brain and spinal cord true Inferred relationship Existential restriction modifier 2
Pelizaeus-Merzbacher disease in female carrier Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Pelizaeus-Merzbacher disease in female carrier Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Pelizaeus-Merzbacher disease in female carrier 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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