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

24210004: Congenital chorioretinal degeneration (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2015. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
40635016 Congenital chorioretinal degeneration en Synonym Active Entire term case insensitive SNOMED CT core module
753821015 Congenital chorioretinal degeneration (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital chorioretinal degeneration Is a Congenital anomaly of posterior segment of eye false Inferred relationship Existential restriction modifier
Congenital chorioretinal degeneration Is a Disorder of choroid of eye false Inferred relationship Existential restriction modifier
Congenital chorioretinal degeneration Is a Congenital degeneration of nervous system false Inferred relationship Existential restriction modifier
Congenital chorioretinal degeneration Is a Chorioretinal disorder false Inferred relationship Existential restriction modifier
Congenital chorioretinal degeneration Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital chorioretinal degeneration Finding site Posterior eyeball segment structure false Inferred relationship Existential restriction modifier 1
Congenital chorioretinal degeneration Finding site Choroidal structure false Inferred relationship Existential restriction modifier 1
Congenital chorioretinal degeneration Finding site Retinal structure false Inferred relationship Existential restriction modifier 1
Congenital chorioretinal degeneration Associated morphology Congenital degeneration false Inferred relationship Existential restriction modifier 1
Congenital chorioretinal degeneration Finding site Structure of nervous system false Inferred relationship Existential restriction modifier
Congenital chorioretinal degeneration Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital chorioretinal degeneration Is a Congenital anomaly of retina true Inferred relationship Existential restriction modifier
Congenital chorioretinal degeneration Is a Congenital anomaly of choroid true Inferred relationship Existential restriction modifier
Congenital chorioretinal degeneration Finding site Retinal structure true Inferred relationship Existential restriction modifier 1
Congenital chorioretinal degeneration Finding site Choroidal structure false Inferred relationship Existential restriction modifier 1
Congenital chorioretinal degeneration Associated morphology Congenital degeneration false Inferred relationship Existential restriction modifier 1
Congenital chorioretinal degeneration Is a Degeneration of retina false Inferred relationship Existential restriction modifier
Congenital chorioretinal degeneration Is a Congenital anomaly of posterior segment of eye false Inferred relationship Existential restriction modifier
Congenital chorioretinal degeneration Is a Disorder of choroid of eye false Inferred relationship Existential restriction modifier
Congenital chorioretinal degeneration Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital chorioretinal degeneration Associated morphology Degeneration false Inferred relationship Existential restriction modifier 2
Congenital chorioretinal degeneration Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Congenital chorioretinal degeneration Associated morphology Degeneration false Inferred relationship Existential restriction modifier 3
Congenital chorioretinal degeneration Finding site Retinal structure false Inferred relationship Existential restriction modifier 2
Congenital chorioretinal degeneration Finding site Choroidal structure false Inferred relationship Existential restriction modifier 3
Congenital chorioretinal degeneration Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Congenital chorioretinal degeneration Finding site Posterior eyeball segment structure false Inferred relationship Existential restriction modifier 2
Congenital chorioretinal degeneration Associated morphology Degeneration false Inferred relationship Existential restriction modifier 4
Congenital chorioretinal degeneration Finding site Retinal structure false Inferred relationship Existential restriction modifier 4
Congenital chorioretinal degeneration Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Congenital chorioretinal degeneration Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital chorioretinal degeneration Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Congenital chorioretinal degeneration Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital chorioretinal degeneration Associated morphology Degeneration false Inferred relationship Existential restriction modifier 1
Congenital chorioretinal degeneration Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 2
Congenital chorioretinal degeneration Finding site Choroidal structure true Inferred relationship Existential restriction modifier 2
Congenital chorioretinal degeneration Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Congenital chorioretinal degeneration Is a Chorioretinal degeneration true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Aicardi's syndrome Is a True Congenital chorioretinal degeneration Inferred relationship Existential restriction modifier
Ectopia lentis, chorioretinal dystrophy, myopia syndrome Is a True Congenital chorioretinal degeneration Inferred relationship Existential restriction modifier
Congenital peripapillary staphyloma Is a True Congenital chorioretinal degeneration Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start