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719166003: Spondyloepimetaphyseal dysplasia matrilin-3 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
3315232012 Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315233019 Spondyloepimetaphyseal dysplasia matrilin-3 type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401989018 A rare primary bone dysplasia due to matrilin-3 variants and characterized by disproportionate early-onset dwarfism, bowing of the lower limbs, short, wide and stocky long bones with severe epiphyseal and metaphyseal changes, lumbar lordosis, hypoplastic iliac bones, flat ovoid vertebral bodies and normal hands. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401990010 A rare primary bone dysplasia due to matrilin-3 variants and characterised by disproportionate early-onset dwarfism, bowing of the lower limbs, short, wide and stocky long bones with severe epiphyseal and metaphyseal changes, lumbar lordosis, hypoplastic iliac bones, flat ovoid vertebral bodies and normal hands. 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 matrilin-3 type (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) Is a Spondyloepimetaphyseal disorder true Inferred relationship Some
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) Occurrence Congenital false Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) Finding site Bone structure false Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) Occurrence Congenital true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) Finding site Bone structure true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) Associated morphology Dysplasia true Inferred relationship Some 1
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Spondyloepimetaphyseal dysplasia matrilin-3 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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