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109471001: Amelogenesis imperfecta, hypocalcification type (disorder)


Status: current, Defined. Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1215860019 Amelogenesis imperfecta - hypomineralisation en Synonym Active Case insensitive SNOMED CT core
1217362017 Amelogenesis imperfecta - hypomineralization en Synonym Active Case insensitive SNOMED CT core
1219482014 Amelogenesis imperfecta - hypocalcified en Synonym Active Case insensitive SNOMED CT core
174045019 Amelogenesis imperfecta, hypocalcification type en Synonym Active Case insensitive SNOMED CT core
612320016 Amelogenesis imperfecta, hypocalcification type (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, hypocalcification type Finding site Enamel structure false Inferred relationship Some 1
Amelogenesis imperfecta, hypocalcification type Pathological process Pathological developmental process true Inferred relationship Some 1
Amelogenesis imperfecta, hypocalcification type Pathological process Pathological developmental process false Inferred relationship Some 2
Amelogenesis imperfecta, hypocalcification type Associated morphology Morphologically abnormal structure false Inferred relationship Some 2
Amelogenesis imperfecta, hypocalcification type Occurrence Congenital true Inferred relationship Some 1
Amelogenesis imperfecta, hypocalcification type Is a Hypomineralisation of enamel of teeth true Inferred relationship Some
Amelogenesis imperfecta, hypocalcification type Finding site Dentition true Inferred relationship Some 2
Amelogenesis imperfecta, hypocalcification type Occurrence Congenital false Inferred relationship Some
Amelogenesis imperfecta, hypocalcification type Has definitional manifestation Hypomineralisation of enamel of tooth false Inferred relationship Some
Amelogenesis imperfecta, hypocalcification type Associated morphology Hypoplasia false Inferred relationship Some 1
Amelogenesis imperfecta, hypocalcification type Finding site Enamel structure false Inferred relationship Some 2
Amelogenesis imperfecta, hypocalcification type Is a Amelogenesis imperfecta true Inferred relationship Some
Amelogenesis imperfecta, hypocalcification type Associated morphology Congenital anomaly false Inferred relationship Some 2
Amelogenesis imperfecta, hypocalcification type Finding site Enamel structure true Inferred relationship Some 1
Amelogenesis imperfecta, hypocalcification type Associated morphology Congenital hypoplasia false Inferred relationship Some 1
Amelogenesis imperfecta, hypocalcification type Finding site Jaw region structure false Inferred relationship Some
Amelogenesis imperfecta, hypocalcification type Associated morphology Hypocalcification false Inferred relationship Some
Amelogenesis imperfecta, hypocalcification type Occurrence Congenital false Inferred relationship Some 3
Amelogenesis imperfecta, hypocalcification type Associated morphology Developmental abnormality false Inferred relationship Some 3
Amelogenesis imperfecta, hypocalcification type Finding site Structure of hard tissue of tooth false Inferred relationship Some 3
Amelogenesis imperfecta, hypocalcification type Occurrence Congenital false Inferred relationship Some 2
Amelogenesis imperfecta, hypocalcification type Finding site Structure of hard tissue of tooth false Inferred relationship Some 2
Amelogenesis imperfecta, hypocalcification type Is a Hypomineralisation of enamel of tooth false Inferred relationship Some
Amelogenesis imperfecta, hypocalcification type Associated morphology Impaired mineralisation true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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