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719201004: Spondyloepimetaphyseal dysplasia Shohat 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
3315399015 Spondyloepimetaphyseal dysplasia Shohat type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3315400010 Spondyloepimetaphyseal dysplasia Shohat type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5401995017 Spondyloepimetaphyseal dysplasia congenita, Shohat type is characterized by severely disproportionate short stature, short limbs, small chest, short neck, thin lips, severe lumbar lordosis, marked genu varum, joint laxity, distended abdomen, mild hepatomegaly and splenomegaly. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401996016 Spondyloepimetaphyseal dysplasia congenita, Shohat type is characterised by severely disproportionate short stature, short limbs, small chest, short neck, thin lips, severe lumbar lordosis, marked genu varum, joint laxity, distended abdomen, mild hepatomegaly and splenomegaly. 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 Shohat type (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Spondyloepimetaphyseal dysplasia Shohat type (disorder) Is a Spondyloepimetaphyseal disorder true Inferred relationship Some
Spondyloepimetaphyseal dysplasia Shohat type (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Spondyloepimetaphyseal dysplasia Shohat type (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Spondyloepimetaphyseal dysplasia Shohat type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia Shohat type (disorder) Occurrence Congenital false Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia Shohat type (disorder) Finding site Bone structure false Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia Shohat type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia Shohat type (disorder) Finding site Bone structure true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia Shohat type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia Shohat type (disorder) Occurrence Congenital true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia Shohat type (disorder) Associated morphology Dysplasia true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia Shohat type (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Spondyloepimetaphyseal dysplasia Shohat type (disorder) Interprets Height / growth measure true Inferred relationship Some 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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