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717823001: Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3323629016 Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3323630014 Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3323631013 Goldblatt chondrodysplasia en Synonym Active Entire term case sensitive SNOMED CT core module
3323632018 Goldblatt syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3323633011 Odontochondrodysplasia 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
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 3
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 3
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 4
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Finding site Tooth structure false Inferred relationship Existential restriction modifier 4
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Is a Metaphyseal chondrodysplasia true Inferred relationship Existential restriction modifier
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Is a Dentinogenesis imperfecta true Inferred relationship Existential restriction modifier
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Finding site Tooth structure false Inferred relationship Existential restriction modifier 1
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Finding site Bone structure true Inferred relationship Existential restriction modifier 2
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 2
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Is a Congenital anomaly of tooth false Inferred relationship Existential restriction modifier
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Is a Developmental hereditary disorder false Inferred relationship Existential restriction modifier
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Interprets Height / growth measure true Inferred relationship Existential restriction modifier 3
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome Finding site Dentin structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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