FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

719041000: Hip dysplasia with enchondromata and ecchondroma syndrome (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
3314766011 Upington disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3314767019 Hip dysplasia with enchondromata and ecchondroma syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3314768012 Hip dysplasia with enchondromata and ecchondroma syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401932017 A rare primary bone dysplasia characterized by Perthes-like pelvic anomalies (premature closure of the capital femoral epiphyses and widened femoral necks with flattened femoral heads), arthralgias of hips and knees, and occurrence of enchondromata and ecchondromata. There have been no further descriptions in the literature since 1971. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401933010 A rare primary bone dysplasia characterised by Perthes-like pelvic anomalies (premature closure of the capital femoral epiphyses and widened femoral necks with flattened femoral heads), arthralgias of hips and knees, and occurrence of enchondromata and ecchondromata. There have been no further descriptions in the literature since 1971. 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
Upington disease Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Upington disease Is a Congenital hip dysplasia true Inferred relationship Some
Upington disease Is a Disorganized development of cartilaginous and fibrous components of the skeleton true Inferred relationship Some
Upington disease Is a Connective tissue hereditary disorder (disorder) true Inferred relationship Some
Upington disease Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Upington disease Associated morphology Congenital dysplasia false Inferred relationship Some 2
Upington disease Occurrence Congenital true Inferred relationship Some 2
Upington disease Finding site Bone structure of acetabulum false Inferred relationship Some 2
Upington disease Associated morphology Congenital dysplasia false Inferred relationship Some 1
Upington disease Finding site Bone structure of acetabulum true Inferred relationship Some 1
Upington disease Occurrence Congenital true Inferred relationship Some 1
Upington disease Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Upington disease Associated morphology Dysplasia true Inferred relationship Some 1
Upington disease Finding site Cartilage structure (body structure) true Inferred relationship Some 2
Upington disease Is a Osteochondropathy true Inferred relationship Some
Upington disease Associated morphology Dysplasia true Inferred relationship Some 2
Upington disease Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Upington disease Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Description inactivation indicator reference set

Back to Start