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109474009: Amelogenesis imperfecta, pigmented hypomaturation type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
174048017 Amelogenesis imperfecta, pigmented hypomaturation type en Synonym Active Entire term case insensitive SNOMED CT core module
612350012 Amelogenesis imperfecta, pigmented hypomaturation type (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amelogenesis imperfecta, pigmented hypomaturation type Is a Amelogenesis imperfecta, hypomaturation type true Inferred relationship Existential restriction modifier
Amelogenesis imperfecta, pigmented hypomaturation type Associated morphology Structure showing abnormal deposition of pigment true Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta, pigmented hypomaturation type Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta, pigmented hypomaturation type Finding site Jaw region structure false Inferred relationship Existential restriction modifier
Amelogenesis imperfecta, pigmented hypomaturation type Finding site Enamel structure false Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta, pigmented hypomaturation type Occurrence Congenital false Inferred relationship Existential restriction modifier
Amelogenesis imperfecta, pigmented hypomaturation type Is a Disorder of pigmentation true Inferred relationship Existential restriction modifier
Amelogenesis imperfecta, pigmented hypomaturation type Is a Degenerative disorder true Inferred relationship Existential restriction modifier
Amelogenesis imperfecta, pigmented hypomaturation type Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta, pigmented hypomaturation type Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Amelogenesis imperfecta, pigmented hypomaturation type Finding site Enamel structure true Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta, pigmented hypomaturation type Finding site Enamel structure false Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta, pigmented hypomaturation type Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Amelogenesis imperfecta, pigmented hypomaturation type Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Amelogenesis imperfecta, pigmented hypomaturation type Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier 3
Amelogenesis imperfecta, pigmented hypomaturation type Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta, pigmented hypomaturation type Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta, pigmented hypomaturation type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta, pigmented hypomaturation type Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta, pigmented hypomaturation type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta, pigmented hypomaturation type Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta, pigmented hypomaturation type Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta, pigmented hypomaturation type Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Amelogenesis imperfecta, pigmented hypomaturation type Is a Oral lesion true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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