FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

707608003: Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder)


Status: current, Primitive. Date: 31-Jan 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3030814014 Jalili syndrome en Synonym Active Case sensitive SNOMED CT core
3030832014 Amelogenesis imperfecta co-occurrent with cone rod dystrophy en Synonym Active Case insensitive SNOMED CT core
3030889013 Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Occurrence Congenital true Inferred relationship Some 1
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Pathological process Pathological developmental process true Inferred relationship Some 1
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Finding site Structure of hard tissue of tooth false Inferred relationship Some 1
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Finding site Enamel structure true Inferred relationship Some 1
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Is a Hereditary retinal dystrophy true Inferred relationship Some
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Is a Amelogenesis imperfecta true Inferred relationship Some
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Associated morphology Dystrophy true Inferred relationship Some 2
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Finding site Retinal structure true Inferred relationship Some 2
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Associated morphology Developmental abnormality false Inferred relationship Some 3
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Occurrence Congenital false Inferred relationship Some 3
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Finding site Structure of hard tissue of tooth false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start