FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

1172696009: Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4635424013 Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4635425014 Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome Is a Autosomal hereditary disorder true Inferred relationship Existential restriction modifier
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome Is a Global developmental delay true Inferred relationship Existential restriction modifier
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome Is a Hereditary cerebellar degeneration true Inferred relationship Existential restriction modifier
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome Is a Visual impairment true Inferred relationship Existential restriction modifier
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome Is a Chronic brain syndrome true Inferred relationship Existential restriction modifier
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome Clinical course Progressive true Inferred relationship Existential restriction modifier 2
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome Finding site Structure of visual system true Inferred relationship Existential restriction modifier 3
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 1
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome Associated morphology Atrophy 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