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783059004: Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3757278012 Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3757279016 Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
3757280018 Atypical dentin dysplasia due to SMOC2 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
3757281019 Dentin dysplasia type 1 with microdontia and shape anomalies 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
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency Finding site Dentin structure true Inferred relationship Existential restriction modifier 1
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency Is a Dentin dysplasia true Inferred relationship Existential restriction modifier
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Atypical dentin dysplasia due to SPARC related modular calcium binding 2 deficiency Is a Developmental hereditary disorder false Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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