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771301002: Axial spondylometaphyseal dysplasia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3705543019 Axial spondylometaphyseal dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3705544013 Axial spondylometaphyseal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3705545014 A rare type of spondylometaphyseal dysplasia with characteristics of metaphyseal changes of the truncal-juxta truncal bones associated with retinal dystrophy. Patients typically present progressive postnatal growth failure with rhizomelic shortening of the limbs, a deformed, hypoplastic thorax and retinitis pigmentosa or pigmentary retinal degeneration. Radiographic findings include short ribs with flared, cupped anterior ends, mild platyspondyly, lacy ilia and metaphyseal dysplasia of the proximal femora. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3705543019 Axial spondylometaphyseal dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3705544013 Axial spondylometaphyseal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3705545014 A rare type of spondylometaphyseal dysplasia with characteristics of metaphyseal changes of the truncal-juxta truncal bones associated with retinal dystrophy. Patients typically present progressive postnatal growth failure with rhizomelic shortening of the limbs, a deformed, hypoplastic thorax and retinitis pigmentosa or pigmentary retinal degeneration. Radiographic findings include short ribs with flared, cupped anterior ends, mild platyspondyly, lacy ilia and metaphyseal dysplasia of the proximal femora. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3382131001000111 Dysplasie, spondyloepimetaphysäre, axiale Form de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
899351000172115 dysplasie spondylo-métaphysaire axiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
899351000172115 dysplasie spondylo-métaphysaire axiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3382131001000111 Dysplasie, spondyloepimetaphysäre, axiale Form de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Axial spondylometaphyseal dysplasia (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Axial spondylometaphyseal dysplasia (disorder) Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept)
Axial spondylometaphyseal dysplasia (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Axial spondylometaphyseal dysplasia (disorder) Is a Metaphyseal chondrodysplasia false Inferred relationship Existential restriction modifier (core metadata concept)
Axial spondylometaphyseal dysplasia (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Axial spondylometaphyseal dysplasia (disorder) Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Axial spondylometaphyseal dysplasia (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Axial spondylometaphyseal dysplasia (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Axial spondylometaphyseal dysplasia (disorder) Is a Spondylometaphyseal dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Axial spondylometaphyseal dysplasia (disorder) Is a Congenital anomaly of skeletal bone false Inferred relationship Existential restriction modifier (core metadata concept)
Axial spondylometaphyseal dysplasia (disorder) Is a Rhizomelic dysplasia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Axial spondylometaphyseal dysplasia (disorder) Interprets Limb length true Inferred relationship Existential restriction modifier (core metadata concept) 2
Axial spondylometaphyseal dysplasia (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Axial spondylometaphyseal dysplasia (disorder) Finding site Bone structure of extremity true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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