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717330004: dysplasie spondylo-épimétaphysaire type Irapa (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3309067015 Spondyloepimetaphyseal dysplasia Irapa type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3309068013 Spondyloepimetaphyseal dysplasia Irapa type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
750961000241114 dysplasie spondylo-épimétaphysaire type Irapa (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
881141000172117 SEMD (spondyloepimetaphyseal dysplasia) type Irapa fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
992341000172115 dysplasie spondylo-épimétaphysaire type Irapa fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3309069017 Syndrome with characteristics of disproportionate short-trunked short stature, pectus carinatum, short arms, short and broad hands, short metatarsals, flat and broad feet, coxa vara, genu valgum, osteoarthritis, arthrosis and moderate-to-serious gait impairment. The syndrome has been described among Venezuelan Indians of the Yukpa (Irapa) tribe and three siblings from a Mexican mestizo family. Autosomal recessive inheritance has been suggested, but the causative gene has not yet been identified. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spondyloepimetaphyseal dysplasia Irapa type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia Irapa type (disorder) morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia Irapa type (disorder) localisation d'une constatation (attribut) structure osseuse true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia Irapa type (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia Irapa type (disorder) morphologie associée (attribut) dysplasie true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia Irapa type (disorder) est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Spondyloepimetaphyseal dysplasia Irapa type (disorder) interprète (attribut) Height / growth measure true Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia Irapa type (disorder) est un(e) (attribut) Autosomal recessive spondyloepimetaphyseal dysplasia false Inferred relationship Some
Spondyloepimetaphyseal dysplasia Irapa type (disorder) morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia Irapa type (disorder) survenue (attribut) congénital false Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia Irapa type (disorder) localisation d'une constatation (attribut) structure osseuse false Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia Irapa type (disorder) est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
Spondyloepimetaphyseal dysplasia Irapa type (disorder) est un(e) (attribut) Spondyloepimetaphyseal disorder true Inferred relationship Some
Spondyloepimetaphyseal dysplasia Irapa type (disorder) est un(e) (attribut) Connective tissue hereditary disorder false Inferred relationship Some
Spondyloepimetaphyseal dysplasia Irapa type (disorder) est un(e) (attribut) Hereditary disorder of musculoskeletal system true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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