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718610008: Congenital pontocerebellar hypoplasia type 1 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3312926017 Congenital pontocerebellar hypoplasia type 1 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3312927014 Congenital pontocerebellar hypoplasia type 1 en Synonym Active Entire term case insensitive SNOMED CT core module
3312928016 PCH1 - pontocerebellar hypoplasia type 1 en Synonym Active Entire term case sensitive SNOMED CT core module
3312929012 Pontocerebellar hypoplasia type 1 en Synonym Active Entire term case insensitive SNOMED CT core module
3312930019 Norman disease en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital pontocerebellar hypoplasia type 1 Is a Congenital pontocerebellar hypoplasia true Inferred relationship Existential restriction modifier
Congenital pontocerebellar hypoplasia type 1 Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Congenital pontocerebellar hypoplasia type 1 Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Congenital pontocerebellar hypoplasia type 1 Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 2
Congenital pontocerebellar hypoplasia type 1 Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital pontocerebellar hypoplasia type 1 Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 2
Congenital pontocerebellar hypoplasia type 1 Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier 3
Congenital pontocerebellar hypoplasia type 1 Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Congenital pontocerebellar hypoplasia type 1 Finding site Pontine structure false Inferred relationship Existential restriction modifier 2
Congenital pontocerebellar hypoplasia type 1 Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 3
Congenital pontocerebellar hypoplasia type 1 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Congenital pontocerebellar hypoplasia type 1 Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 1 Finding site Pontine structure true Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 1 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 1 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 1 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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