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59636002: Pelizaeus-Merzbacher disease, connatal variant (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
1231984012 Type II congenital Pelizaeus-Merzbacher disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
798500019 Pelizaeus-Merzbacher disease, connatal variant (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
99071013 Pelizaeus-Merzbacher disease, connatal variant en Synonym (core metadata concept) 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
Pelizaeus-Merzbacher disease, connatal variant (disorder) est un(e) (attribut) Congenital degeneration of nervous system true Inferred relationship Some
Pelizaeus-Merzbacher disease, connatal variant (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Pelizaeus-Merzbacher disease, connatal variant (disorder) est un(e) (attribut) Congenital anomaly of central nervous system true Inferred relationship Some
Pelizaeus-Merzbacher disease, connatal variant (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Pelizaeus-Merzbacher disease, connatal variant (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) est un(e) (attribut) X-linked recessive hereditary disease true Inferred relationship Some
Pelizaeus-Merzbacher disease, connatal variant (disorder) est un(e) (attribut) Pelizaeus-Merzbacher disease true Inferred relationship Some
Pelizaeus-Merzbacher disease, connatal variant (disorder) morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) morphologie associée (attribut) Myelin sheath alteration false Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) morphologie associée (attribut) Myelin sheath alteration true Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) localisation d'une constatation (attribut) système nerveux false Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) morphologie associée (attribut) Sudanophilic stain reaction false Inferred relationship Some 3
Pelizaeus-Merzbacher disease, connatal variant (disorder) survenue (attribut) congénital false Inferred relationship Some 4
Pelizaeus-Merzbacher disease, connatal variant (disorder) localisation d'une constatation (attribut) système nerveux false Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) morphologie associée (attribut) Dystrophy (morphologic abnormality) true Inferred relationship Some 2
Pelizaeus-Merzbacher disease, connatal variant (disorder) localisation d'une constatation (attribut) Myelinated nerve fiber structure true Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) localisation d'une constatation (attribut) White matter structure of brain and spinal cord (body structure) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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