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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
99071013 Pelizaeus-Merzbacher disease, connatal variant en Synonym (core metadata concept) Active Entire term case sensitive (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
1231984012 Type II congenital Pelizaeus-Merzbacher disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2672821000005113 Pelizaeus-Merzbachers sygdom, konnatal variant da Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) dansk modul


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pelizaeus-Merzbacher disease, connatal variant (disorder) Is a Pelizaeus-Merzbacher disease (disorder) true Inferred relationship Some
Pelizaeus-Merzbacher disease, connatal variant (disorder) Associated morphology Sudanophilic stain reaction false Inferred relationship Some 3
Pelizaeus-Merzbacher disease, connatal variant (disorder) Occurrence Congenital false Inferred relationship Some 4
Pelizaeus-Merzbacher disease, connatal variant (disorder) Finding site Structure of nervous system (body structure) false Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) Associated morphology Dystrophy false Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) Associated morphology Myelin sheath alteration false Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) Associated morphology Myelin sheath alteration true Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) Associated morphology Dystrophy false Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) Finding site Structure of nervous system (body structure) false Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) Associated morphology Dystrophy true Inferred relationship Some 2
Pelizaeus-Merzbacher disease, connatal variant (disorder) Finding site Myelinated nerve fiber structure true Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) Finding site White matter structure of brain and spinal cord (body structure) true Inferred relationship Some 2
Pelizaeus-Merzbacher disease, connatal variant (disorder) Is a Congenital degeneration of nervous system true Inferred relationship Some
Pelizaeus-Merzbacher disease, connatal variant (disorder) Occurrence Congenital true Inferred relationship Some 1
Pelizaeus-Merzbacher disease, connatal variant (disorder) Occurrence Congenital true Inferred relationship Some 2
Pelizaeus-Merzbacher disease, connatal variant (disorder) Is a 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) Is a X-linked recessive hereditary disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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