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785818007: Structure of joint region (body structure)

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

Descriptions:

Id Description Lang Type Status Case? Module
3768577019 Structure of joint region en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3768578012 Structure of joint region (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3768577019 Structure of joint region en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3768578012 Structure of joint region (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5738 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Structure of joint region Is a Body region structure true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Familial normophosphatemic tumoral calcinosis Finding site False Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 2
Tumoral calcinosis Finding site False Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperphosphatemic familial tumoral calcinosis (disorder) Finding site False Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 2
Prenatal-onset spinal muscular atrophy with congenital bone fractures Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 1
NIMA related kinase 9 lethal skeletal dysplasia (disorder) Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 2
Spondyloepiphyseal dysplasia Stanescu type Finding site False Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 3
Myosin binding protein C1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome (disorder) Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 2
Myopathic Ehlers-Danlos syndrome (disorder) Finding site False Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 4
Antenatal multi-minicore disease with arthrogryposis multiplex congenita Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 2
Diastrophic dysplasia Finding site False Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 3
A group of disorders with characteristics of congenital limb contractures manifesting as limitation of movement of multiple limb joints at birth that is usually non-progressive and may include muscle weakness and fibrosis. This disorder is always associated with decreased intrauterine fetal movement, which leads secondarily to the contractures. Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 1
Pena-Shokeir syndrome type I (disorder) Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 1
Marden Walker syndrome (disorder) Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 2
Microphthalmia, microtia, fetal akinesia syndrome Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 6
Hecht syndrome Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital muscular dystrophy with arthrogryposis multiplex congenita Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital amyoplasia Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial normophosphatemic tumoral calcinosis Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 1
Tumoral calcinosis Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperphosphatemic familial tumoral calcinosis (disorder) Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pontocerebellar hypoplasia type 12 Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 5
Progressive flexion contracture of joint (disorder) Finding site True Structure of joint region Inferred relationship Existential restriction modifier (core metadata concept) 1

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

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