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717330004: Spondyloepimetaphyseal dysplasia Irapa type (disorder)


Status: current, Primitive. 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 Initial character case insensitive SNOMED CT core
3309068013 Spondyloepimetaphyseal dysplasia Irapa type en Synonym Active Initial character case insensitive SNOMED CT core
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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spondyloepimetaphyseal dysplasia Irapa type Pathological process Pathological developmental process true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia Irapa type Associated morphology Congenital dysplasia false Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia Irapa type Finding site Bone structure true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia Irapa type Occurrence Congenital true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia Irapa type Associated morphology Dysplasia true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia Irapa type Is a Developmental hereditary disorder true Inferred relationship Some
Spondyloepimetaphyseal dysplasia Irapa type Interprets Height / growth measure true Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia Irapa type Is a Autosomal recessive spondyloepimetaphyseal dysplasia false Inferred relationship Some
Spondyloepimetaphyseal dysplasia Irapa type Associated morphology Congenital dysplasia false Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia Irapa type Occurrence Congenital false Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia Irapa type Finding site Bone structure false Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia Irapa type Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Spondyloepimetaphyseal dysplasia Irapa type Is a Spondyloepimetaphyseal disorder true Inferred relationship Some
Spondyloepimetaphyseal dysplasia Irapa type Is a Inherited disorder of connective tissue false Inferred relationship Some
Spondyloepimetaphyseal dysplasia Irapa type Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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