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719165004: Spondyloepimetaphyseal dysplasia aggrecan type (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3315229014 Spondyloepimetaphyseal dysplasia aggrecan type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315230016 Spondyloepimetaphyseal dysplasia aggrecan type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401987016 Spondyloepimetaphyseal dysplasia, aggrecan type is a new form of skeletal dysplasia characterized by severe short stature, facial dysmorphism and characteristic radiographic findings. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401988014 Spondyloepimetaphyseal dysplasia, aggrecan type is a new form of skeletal dysplasia characterised by severe short stature, facial dysmorphism and characteristic radiographic findings. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3315229014 Spondyloepimetaphyseal dysplasia aggrecan type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3315229014 Spondyloepimetaphyseal dysplasia aggrecan type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315230016 Spondyloepimetaphyseal dysplasia aggrecan type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3315230016 Spondyloepimetaphyseal dysplasia aggrecan type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315231017 A new form of skeletal dysplasia with manifestations of severe short stature, facial dysmorphism and characteristic radiographic findings. To date, three cases have been described, all originating from the same family. The disease results from a missense mutation affecting the C-type lectin domain of aggrecan (AGC1 gene; chromosome 15) which regulates endochondral ossification. Transmission is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401987016 Spondyloepimetaphyseal dysplasia, aggrecan type is a new form of skeletal dysplasia characterized by severe short stature, facial dysmorphism and characteristic radiographic findings. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401988014 Spondyloepimetaphyseal dysplasia, aggrecan type is a new form of skeletal dysplasia characterised by severe short stature, facial dysmorphism and characteristic radiographic findings. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3385391001000118 Dysplasie, spondyloepimetaphysäre, Typ Aggrecan de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
880761000172114 dysplasie spondylo-épimétaphysaire type aggrécane fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
961491000172114 SEMD (pondyloepimetaphyseal dysplasia) type aggrécane fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
880761000172114 dysplasie spondylo-épimétaphysaire type aggrécane fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
961491000172114 SEMD (pondyloepimetaphyseal dysplasia) type aggrécane fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3385391001000118 Dysplasie, spondyloepimetaphysäre, Typ Aggrecan de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spondyloepimetaphyseal dysplasia aggrecan type (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepimetaphyseal dysplasia aggrecan type (disorder) Is a Spondyloepimetaphyseal disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepimetaphyseal dysplasia aggrecan type (disorder) Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepimetaphyseal dysplasia aggrecan type (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepimetaphyseal dysplasia aggrecan type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Spondyloepimetaphyseal dysplasia aggrecan type (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Spondyloepimetaphyseal dysplasia aggrecan type (disorder) Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Spondyloepimetaphyseal dysplasia aggrecan type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepimetaphyseal dysplasia aggrecan type (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepimetaphyseal dysplasia aggrecan type (disorder) Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepimetaphyseal dysplasia aggrecan type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepimetaphyseal dysplasia aggrecan type (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepimetaphyseal dysplasia aggrecan type (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepimetaphyseal dysplasia aggrecan type (disorder) Interprets Height / growth measure (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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