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715436007: Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (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
3302596011 Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3302599016 Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration en Synonym Active Entire term case insensitive SNOMED CT core module
3302623015 Cerebellar hypoplasia and tapetoretinal degeneration 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
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Is a Congenital cerebellar hypoplasia true Inferred relationship Existential restriction modifier
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Finding site Structure of visual system false Inferred relationship Existential restriction modifier
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier 2
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 2
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Finding site Structure of visual system true Inferred relationship Existential restriction modifier 2
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 1
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 1
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration 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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