FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

234962001: Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth (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
352125013 Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth en Synonym Active Entire term case insensitive SNOMED CT core module
623350018 Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth (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 - hypoplastic autosomal dominant - smooth Is a Amelogenesis imperfecta, hypoplastic type true Inferred relationship Existential restriction modifier
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Enamel structure true Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Jaw region structure false Inferred relationship Existential restriction modifier
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Occurrence Congenital false Inferred relationship Existential restriction modifier
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Enamel structure false Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Enamel structure false Inferred relationship Existential restriction modifier 2
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier 3
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start