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707608003: amelogenesis imperfecta gelijktijdig met kegel-staafdystrofie (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3030814014 Jalili syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3030832014 Amelogenesis imperfecta co-occurrent with cone rod dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3030889013 Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6485061000146117 amelogenesis imperfecta gelijktijdig met kegel-staafdystrofie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6485071000146111 amelogenesis imperfecta gelijktijdig met kegel-staafdystrofie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7311691000146112 syndroom van Jalili nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
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 (disorder) 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 gebrekkige ontwikkeling (afwijkende morfologie) 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
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 (attribute) Pathological developmental process true Inferred relationship Some 1
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Associated morphology Morphologically abnormal structure (morphologic abnormality) 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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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