FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

1156796002: Autosomal dominant cerebellar ataxia type 2 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4576206010 Autosomal dominant cerebellar ataxia type 2 en Synonym Active Entire term case insensitive SNOMED CT core module
4576207018 Autosomal dominant cerebellar ataxia type 2 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant cerebellar ataxia type 2 Is a Cerebellar ataxia true Inferred relationship Existential restriction modifier
Autosomal dominant cerebellar ataxia type 2 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant cerebellar ataxia type 2 Is a Hereditary ataxia true Inferred relationship Existential restriction modifier
Autosomal dominant cerebellar ataxia type 2 Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start