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718393002: Atypical Rett syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3306452010 Atypical Rett syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3312131019 Atypical Rett syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Atypical Rett syndrome Is a Hereditary disease false Inferred relationship Existential restriction modifier
Atypical Rett syndrome Is a Pervasive developmental disorder true Inferred relationship Existential restriction modifier
Atypical Rett syndrome Is a X-linked hereditary disease true Inferred relationship Existential restriction modifier
Atypical Rett syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Atypical Rett syndrome Is a Developmental hereditary disorder 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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