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109474009: Amelogenesis imperfecta, pigmented hypomaturation type (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
174048017 Amelogenesis imperfecta, pigmented hypomaturation type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
612350012 Amelogenesis imperfecta, pigmented hypomaturation type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
174048017 Amelogenesis imperfecta, pigmented hypomaturation type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
174048017 Amelogenesis imperfecta, pigmented hypomaturation type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
612350012 Amelogenesis imperfecta, pigmented hypomaturation type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
612350012 Amelogenesis imperfecta, pigmented hypomaturation type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
126371000077111 amélogénèse imparfaite de type hypomaturation pigmentée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
126371000077111 amélogénèse imparfaite de type hypomaturation pigmentée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Is a Amelogenesis imperfecta, hypomaturation type (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Associated morphology Structure showing abnormal deposition of pigment (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Finding site Jaw region structure false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Finding site Enamel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Is a Disorder of pigmentation (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Is a Degenerative disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Finding site Enamel structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Finding site Enamel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Is a Oral lesion (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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