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707607008: Amelogenesis imperfecta and gingival hyperplasia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2015. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3030774014 Amelogenesis imperfecta and gingival hyperplasia syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3030784010 Amelogenesis imperfecta and gingival hyperplasia syndrome en Synonym 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 and gingival hyperplasia syndrome Is a Amelogenesis imperfecta true Inferred relationship Existential restriction modifier
Amelogenesis imperfecta and gingival hyperplasia syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Amelogenesis imperfecta and gingival hyperplasia syndrome Is a Gingivae finding false Inferred relationship Existential restriction modifier
Amelogenesis imperfecta and gingival hyperplasia syndrome Is a Hyperplasia of gingiva true Inferred relationship Existential restriction modifier
Amelogenesis imperfecta and gingival hyperplasia syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Amelogenesis imperfecta and gingival hyperplasia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Amelogenesis imperfecta and gingival hyperplasia syndrome Finding site Structure of hard tissue of tooth false Inferred relationship Existential restriction modifier 2
Amelogenesis imperfecta and gingival hyperplasia syndrome Associated morphology Hyperplasia false Inferred relationship Existential restriction modifier 3
Amelogenesis imperfecta and gingival hyperplasia syndrome Finding site Gingival structure false Inferred relationship Existential restriction modifier 3
Amelogenesis imperfecta and gingival hyperplasia syndrome Associated morphology Hyperplasia true Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta and gingival hyperplasia syndrome Finding site Gingival structure true Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta and gingival hyperplasia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Amelogenesis imperfecta and gingival hyperplasia syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Amelogenesis imperfecta and gingival hyperplasia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta and gingival hyperplasia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Amelogenesis imperfecta and gingival hyperplasia syndrome Finding site Enamel structure true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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