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707607008: Amelogenesis imperfecta and gingival hyperplasia syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3030774014 Amelogenesis imperfecta and gingival hyperplasia syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3030784010 Amelogenesis imperfecta and gingival hyperplasia syndrome en Synonym Active Case insensitive SNOMED CT core
3030936011 Associates gingival fibromatosis with dental abnormalities including generalized thin hypoplastic amelogenesis imperfecta, intrapulpal calcifications and delay of tooth eruption. en Definition Active Case sensitive SNOMED CT core
3030939016 Associates gingival fibromatosis with dental abnormalities including generalised thin hypoplastic amelogenesis imperfecta, intrapulpal calcifications and delay of tooth eruption. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amelogenesis imperfecta and gingival hyperplasia syndrome Associated morphology Hyperplasia true Inferred relationship Some 1
Amelogenesis imperfecta and gingival hyperplasia syndrome Finding site Gingival structure true Inferred relationship Some 1
Amelogenesis imperfecta and gingival hyperplasia syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Amelogenesis imperfecta and gingival hyperplasia syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Amelogenesis imperfecta and gingival hyperplasia syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Amelogenesis imperfecta and gingival hyperplasia syndrome Occurrence Congenital true Inferred relationship Some 1
Amelogenesis imperfecta and gingival hyperplasia syndrome Finding site Enamel structure true Inferred relationship Some 2
Amelogenesis imperfecta and gingival hyperplasia syndrome Is a Amelogenesis imperfecta true Inferred relationship Some
Amelogenesis imperfecta and gingival hyperplasia syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Amelogenesis imperfecta and gingival hyperplasia syndrome Is a Gingivae finding false Inferred relationship Some
Amelogenesis imperfecta and gingival hyperplasia syndrome Is a Hyperplasia of gingiva true Inferred relationship Some
Amelogenesis imperfecta and gingival hyperplasia syndrome Associated morphology Developmental abnormality false Inferred relationship Some 2
Amelogenesis imperfecta and gingival hyperplasia syndrome Occurrence Congenital true Inferred relationship Some 2
Amelogenesis imperfecta and gingival hyperplasia syndrome Finding site Structure of hard tissue of tooth false Inferred relationship Some 2
Amelogenesis imperfecta and gingival hyperplasia syndrome Associated morphology Hyperplasia false Inferred relationship Some 3
Amelogenesis imperfecta and gingival hyperplasia syndrome Finding site Gingival structure false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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