FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.1  |  FHIR Version n/a  User: [n/a]

78494001: Amelogenesis imperfecta (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
130245014 Amelogenesis imperfecta en Synonym Active Entire term case insensitive SNOMED CT core module
130246010 Congenital enamel hypoplasia en Synonym Active Entire term case insensitive SNOMED CT core module
503854013 AI - Amelogenesis imperfecta en Synonym Active Entire term case sensitive SNOMED CT core module
819440011 Amelogenesis imperfecta (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

22 descendants. Search Descendants:

Expanded Value Set

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

This concept is not in any reference sets

Back to Start