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773303005: Spondyloepimetaphyseal dysplasia Genevieve type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3723047017 Spondyloepimetaphyseal dysplasia Genevieve type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3723048010 Spondyloepimetaphyseal dysplasia Geneviève type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3723049019 Spondyloepimetaphyseal dysplasia Genevieve type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3723050019 SEMDG - spondyloepimetaphyseal dysplasia Genevieve type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3723052010 A rare primary bone dysplasia with characteristics of severe developmental delay and skeletal dysplasia (including short stature, premature carpal ossification, platyspondyly, longitudinal metaphyseal striations, and small epiphyses), as well as moderate to severe intellectual disability and facial dysmorphism, including prominent forehead, mild synophrys, depressed nasal bridge, prominent bulbous nasal tip and full lips. Caused by homozygous or compound heterozygous mutation in the NANS gene on chromosome 9q22. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3723047017 Spondyloepimetaphyseal dysplasia Genevieve type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3723048010 Spondyloepimetaphyseal dysplasia Geneviève type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3723049019 Spondyloepimetaphyseal dysplasia Genevieve type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3723050019 SEMDG - spondyloepimetaphyseal dysplasia Genevieve type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3723052010 A rare primary bone dysplasia with characteristics of severe developmental delay and skeletal dysplasia (including short stature, premature carpal ossification, platyspondyly, longitudinal metaphyseal striations, and small epiphyses), as well as moderate to severe intellectual disability and facial dysmorphism, including prominent forehead, mild synophrys, depressed nasal bridge, prominent bulbous nasal tip and full lips. Caused by homozygous or compound heterozygous mutation in the NANS gene on chromosome 9q22. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3392641001000114 Dysplasie, spondyloepimetaphysäre, Typ Geneviève de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
932501000172118 SEMD (spondyloepimetaphyseal dysplasia) type Geneviève fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1002761000172110 dysplasie spondylo-épimétaphysaire type Geneviève fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
932501000172118 SEMD (spondyloepimetaphyseal dysplasia) type Geneviève fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1002761000172110 dysplasie spondylo-épimétaphysaire type Geneviève fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3392641001000114 Dysplasie, spondyloepimetaphysäre, Typ Geneviève 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 Genevieve type (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Is a Spondyloepimetaphyseal disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Is a Intelligenzminderung true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Is a Developmental delay true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Finding site Face structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 2
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Interprets Height / growth measure (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Interprets Intellectual ability (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Interprets Adaptation behavior true Inferred relationship Existential restriction modifier (core metadata concept) 5
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 5

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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