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109474009: Amelogenesis imperfecta, pigmented hypomaturation type (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
174048017 Amelogenesis imperfecta, pigmented hypomaturation type en Synonym Active Case insensitive SNOMED CT core
612350012 Amelogenesis imperfecta, pigmented hypomaturation 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, pigmented hypomaturation type Finding site Enamel structure false Inferred relationship Some 1
Amelogenesis imperfecta, pigmented hypomaturation type Finding site Structure of hard tissue of tooth false Inferred relationship Some 1
Amelogenesis imperfecta, pigmented hypomaturation type Occurrence Congenital true Inferred relationship Some 1
Amelogenesis imperfecta, pigmented hypomaturation type Associated morphology Morphologically abnormal structure false Inferred relationship Some 1
Amelogenesis imperfecta, pigmented hypomaturation type Pathological process Pathological developmental process true Inferred relationship Some 1
Amelogenesis imperfecta, pigmented hypomaturation type Associated morphology Morphologically abnormal structure false Inferred relationship Some 1
Amelogenesis imperfecta, pigmented hypomaturation type Pathological process Pathological developmental process false Inferred relationship Some 1
Amelogenesis imperfecta, pigmented hypomaturation type Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Amelogenesis imperfecta, pigmented hypomaturation type Is a Oral lesion true Inferred relationship Some
Amelogenesis imperfecta, pigmented hypomaturation type Occurrence Congenital false Inferred relationship Some
Amelogenesis imperfecta, pigmented hypomaturation type Is a Disorder of pigmentation true Inferred relationship Some
Amelogenesis imperfecta, pigmented hypomaturation type Is a Degenerative disorder true Inferred relationship Some
Amelogenesis imperfecta, pigmented hypomaturation type Associated morphology Hypoplasia false Inferred relationship Some 1
Amelogenesis imperfecta, pigmented hypomaturation type Is a Amelogenesis imperfecta, hypomaturation type true Inferred relationship Some
Amelogenesis imperfecta, pigmented hypomaturation type Associated morphology Congenital anomaly false Inferred relationship Some 2
Amelogenesis imperfecta, pigmented hypomaturation type Finding site Enamel structure true Inferred relationship Some 1
Amelogenesis imperfecta, pigmented hypomaturation type Finding site Enamel structure false Inferred relationship Some 1
Amelogenesis imperfecta, pigmented hypomaturation type Associated morphology Pigment deposition true Inferred relationship Some 1
Amelogenesis imperfecta, pigmented hypomaturation type Associated morphology Congenital hypoplasia false Inferred relationship Some 1
Amelogenesis imperfecta, pigmented hypomaturation type Finding site Jaw region structure false Inferred relationship Some
Amelogenesis imperfecta, pigmented hypomaturation type Occurrence Congenital false Inferred relationship Some 3
Amelogenesis imperfecta, pigmented hypomaturation type Associated morphology Developmental abnormality false Inferred relationship Some 3
Amelogenesis imperfecta, pigmented hypomaturation type Finding site Structure of hard tissue of tooth false Inferred relationship Some 3
Amelogenesis imperfecta, pigmented hypomaturation type Occurrence Congenital false 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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