FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

34643004: Diaphyseal dysplasia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
57824015 Diaphyseal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
57825019 Engelmann's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
57826018 Diaphyseal sclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
57827010 Osteopathia hyperostotica multiplex infantis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
485906010 Engelmann syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
485907018 Engelman's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
485908011 Camurati-Engelmann syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
766191016 Diaphyseal dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4592854016 Progressive diaphyseal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4592855015 A rare clinically variable bone dysplasia syndrome with characteristics of hyperostosis of the long bones, skull, spine and pelvis, associated with severe pain in the extremities, a wide-based waddling gait, joint contractures, muscle weakness and easy fatigability. In more than 90% of patients, mutations in the transforming growth factor TGFB1 gene (19q13.1) are detected. Inherited as an autosomal dominant trait with reduced penetrance. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
1953821000052110 diafyseal dysplasi sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Diaphyseal dysplasia Is a Disorder of bone and articular cartilage false Inferred relationship Some
Diaphyseal dysplasia Is a Congenital anomaly of cartilage false Inferred relationship Some
Diaphyseal dysplasia Is a Osteochondrodysplasia syndrome false Inferred relationship Some
Diaphyseal dysplasia Is a Dysplasia with increased bone density (disorder) true Inferred relationship Some
Diaphyseal dysplasia Finding site Structure of diaphysis (body structure) false Inferred relationship Some 1
Diaphyseal dysplasia Finding site broskvävnad, struktur false Inferred relationship Some
Diaphyseal dysplasia Finding site Skeletal system structure false Inferred relationship Some 1
Diaphyseal dysplasia Associated morphology Dysplasia true Inferred relationship Some 1
Diaphyseal dysplasia Occurrence Congenital false Inferred relationship Some
Diaphyseal dysplasia Associated morphology kongenital dysplasi false Inferred relationship Some 1
Diaphyseal dysplasia Is a Disorder of bone (disorder) false Inferred relationship Some
Diaphyseal dysplasia Is a Skeletal dysplasia false Inferred relationship Some
Diaphyseal dysplasia Occurrence Congenital false Inferred relationship Some
Diaphyseal dysplasia Is a Congenital malformation false Inferred relationship Some
Diaphyseal dysplasia Is a Disorder of bone (disorder) false Inferred relationship Some
Diaphyseal dysplasia Is a Congenital connective tissue disorder false Inferred relationship Some
Diaphyseal dysplasia Finding site Bone structure false Inferred relationship Some
Diaphyseal dysplasia Is a Skeletal dysplasia false Inferred relationship Some
Diaphyseal dysplasia Finding site Structure of diaphysis (body structure) false Inferred relationship Some 1
Diaphyseal dysplasia Associated morphology kongenital dysplasi false Inferred relationship Some 1
Diaphyseal dysplasia Occurrence Congenital false Inferred relationship Some 2
Diaphyseal dysplasia Associated morphology kongenital dysplasi false Inferred relationship Some 2
Diaphyseal dysplasia Finding site Structure of diaphysis (body structure) false Inferred relationship Some 2
Diaphyseal dysplasia Associated morphology kongenital dysplasi false Inferred relationship Some 1
Diaphyseal dysplasia Occurrence Congenital true Inferred relationship Some 1
Diaphyseal dysplasia Finding site Structure of diaphysis (body structure) true Inferred relationship Some 1
Diaphyseal dysplasia Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Diaphyseal dysplasia Is a fynd som rör kroppsregion false Inferred relationship Some
Diaphyseal dysplasia Is a Congenital anomaly of skeletal bone true Inferred relationship Some
Diaphyseal dysplasia Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Diaphyseal dysplasia Is a Chronic disease of musculoskeletal system true Inferred relationship Some
Diaphyseal dysplasia Is a Developmental hereditary disorder true Inferred relationship Some
Diaphyseal dysplasia Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Diaphyseal dysplasia Clinical course Progressive (qualifier value) true Inferred relationship Some 3
Diaphyseal dysplasia Interprets Bone density scan true Inferred relationship Some 2
Diaphyseal dysplasia Has interpretation Above reference range true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Ghosal hematodiaphyseal dysplasia Is a False Diaphyseal dysplasia Inferred relationship Some
progressiv diafyseal dysplasi Is a False Diaphyseal dysplasia Inferred relationship Some

This concept is not in any reference sets

Back to Start