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719171005: Spondyloepimetaphyseal dysplasia Missouri type (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3315249017 Spondyloepimetaphyseal dysplasia Missouri type (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3315250017 Spondyloepimetaphyseal dysplasia Missouri type en Synonym Active Initial character case insensitive SNOMED CT core
3315251018 Spondyloepimetaphyseal dysplasia type 2 en Synonym Active Case insensitive SNOMED CT core
3315252013 Disorder with manifestations of moderate-to-severe metaphyseal changes, mild epiphyseal involvement, rhizomelic shortening of the lower limbs with bowing of the femora and/or tibiae, coxa vara, genu varum and pear-shaped vertebrae in childhood. The syndrome has been described in a large Missouri (US) kindred with 14 affected members in 4 generations. Though some spontaneous improvement of the skeletal defects may occur in adolescence, the affected individuals remained shorter than their age-matched unaffected siblings. Predisposition deformities to osteoarthritis have been noted. This condition is caused by mutation in the MMP13 gene (locus 11q22.3) and transmitted in an autosomal dominant manner. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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