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78494001: Amelogenesis imperfecta (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
130245014 Amelogenesis imperfecta en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
130246010 Congenital enamel hypoplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
503854013 AI - Amelogenesis imperfecta en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
819440011 Amelogenesis imperfecta (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
130245014 Amelogenesis imperfecta en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
130245014 Amelogenesis imperfecta en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
130246010 Congenital enamel hypoplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
130246010 Congenital enamel hypoplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
503854013 AI - Amelogenesis imperfecta en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
819440011 Amelogenesis imperfecta (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
819440011 Amelogenesis imperfecta (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3393081001000116 Amelogenesis imperfecta de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
872431000172115 amélogenèse imparfaite fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
872431000172115 amélogenèse imparfaite fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3393081001000116 Amelogenesis imperfecta de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

23 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amelogenesis imperfecta (disorder) Is a Hereditary or idiopathic disturbance of tooth structure false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta (disorder) Is a Enamel hypoplasia (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta (disorder) Finding site Enamel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta (disorder) Finding site Jaw region structure false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta (disorder) Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta (disorder) Is a Congenital anomaly of digestive tract false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta (disorder) Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta (disorder) Is a Congenital anomaly of teeth false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta (disorder) Is a Congenital anomaly of tooth (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta (disorder) Is a Congenital anomaly of jaw (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta (disorder) Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Amelogenesis imperfecta (disorder) Finding site Enamel structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta (disorder) Finding site Enamel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Amelogenesis imperfecta (disorder) Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta (disorder) Is a Disorder of hard tissues of teeth (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta (disorder) Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta (disorder) Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta (disorder) Is a Hereditary disorder of tooth true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Amelogenesis imperfecta, hypocalcification type Is a True Amelogenesis imperfecta (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta, hypomaturation type (disorder) Is a True Amelogenesis imperfecta (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta, hypoplastic type Is a True Amelogenesis imperfecta (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Enamel-renal syndrome Is a True Amelogenesis imperfecta (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta, intellectual disability, and epileptic seizures. Is a True Amelogenesis imperfecta (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Agenesis of enamel Is a True Amelogenesis imperfecta (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Is a True Amelogenesis imperfecta (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Amelogenesis imperfecta and gingival hyperplasia syndrome (disorder) Is a True Amelogenesis imperfecta (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome (disorder) Is a True Amelogenesis imperfecta (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Trichodysplasia with amelogenesis imperfecta syndrome (disorder) Is a True Amelogenesis imperfecta (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome (disorder) Is a True Amelogenesis imperfecta (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Late-onset localized junctional epidermolysis bullosa, intellectual disability syndrome (disorder) Is a True Amelogenesis imperfecta (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome (disorder) Is a True Amelogenesis imperfecta (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome (disorder) Is a True Amelogenesis imperfecta (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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