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109494000: Dentin dysplasia, type II (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1219491013 Dentine dysplasia - Shield's type II en Synonym Active Initial character case insensitive SNOMED CT core
1219492018 Anomalous dysplasia of dentine en Synonym Active Case insensitive SNOMED CT core
1219493011 Coronal dentine dysplasia en Synonym Active Case insensitive SNOMED CT core
1219494017 Pulpal dysplasia en Synonym Active Case insensitive SNOMED CT core
174072010 Dentin dysplasia, type II en Synonym Active Initial character case insensitive SNOMED CT core
612561017 Dentin dysplasia, type II (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dentin dysplasia, type II Occurrence Congenital true Inferred relationship Some 1
Dentin dysplasia, type II Pathological process Pathological developmental process true Inferred relationship Some 1
Dentin dysplasia, type II Is a Developmental hereditary disorder false Inferred relationship Some
Dentin dysplasia, type II Is a Dentin dysplasia true Inferred relationship Some
Dentin dysplasia, type II Is a Disorder of hard tissues of teeth false Inferred relationship Some
Dentin dysplasia, type II Finding site Face structure false Inferred relationship Some
Dentin dysplasia, type II Finding site Oral cavity structure false Inferred relationship Some 4
Dentin dysplasia, type II Finding site Tooth structure false Inferred relationship Some 2
Dentin dysplasia, type II Finding site Digestive organ structure false Inferred relationship Some 1
Dentin dysplasia, type II Finding site Upper aerodigestive tract structure false Inferred relationship Some
Dentin dysplasia, type II Is a Congenital anomaly of tooth false Inferred relationship Some
Dentin dysplasia, type II Associated morphology Dysplasia true Inferred relationship Some 1
Dentin dysplasia, type II Finding site Dentin structure true Inferred relationship Some 1
Dentin dysplasia, type II Associated morphology Congenital anomaly false Inferred relationship Some 2
Dentin dysplasia, type II Finding site Tooth structure false Inferred relationship Some 2
Dentin dysplasia, type II Is a Congenital anomaly of teeth false Inferred relationship Some
Dentin dysplasia, type II Is a Digestive system hereditary disorder false Inferred relationship Some
Dentin dysplasia, type II Is a Autosomal dominant hereditary disorder false Inferred relationship Some
Dentin dysplasia, type II Occurrence Congenital false Inferred relationship Some
Dentin dysplasia, type II Associated morphology Congenital anomaly false Inferred relationship Some 2
Dentin dysplasia, type II Finding site Jaw region structure false Inferred relationship Some
Dentin dysplasia, type II Finding site Tooth structure false Inferred relationship Some 2
Dentin dysplasia, type II Associated morphology Congenital malformation false Inferred relationship Some 4
Dentin dysplasia, type II Finding site Tongue structure false Inferred relationship Some
Dentin dysplasia, type II Associated morphology Dysplasia false Inferred relationship Some 1
Dentin dysplasia, type II Finding site Dentin structure false Inferred relationship Some 1
Dentin dysplasia, type II Associated morphology Developmental abnormality false Inferred relationship Some 1
Dentin dysplasia, type II Occurrence Congenital false Inferred relationship Some 3
Dentin dysplasia, type II Associated morphology Developmental abnormality false Inferred relationship Some 3
Dentin dysplasia, type II Finding site Tooth structure false Inferred relationship Some 3
Dentin dysplasia, type II Is a Oral lesion false Inferred relationship Some
Dentin dysplasia, type II Is a Lesion of face false Inferred relationship Some

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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