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732248005: Coxoauricular syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3464715017 Coxoauricular syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3464716016 Coxoauricular syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5403617015 A rare primary bone defect, described only in a mother and her three daughters to date, characterized by short stature, hip dislocation, minor vertebral and pelvic changes, and microtia with hearing loss. There have been no further descriptions in the literature since 1981. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403618013 A rare primary bone defect, described only in a mother and her three daughters to date, characterised by short stature, hip dislocation, minor vertebral and pelvic changes, and microtia with hearing loss. There have been no further descriptions in the literature since 1981. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3464715017 Coxoauricular syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3464716016 Coxoauricular syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3464717013 An extremely rare primary bone defect described only in a mother and her three daughters to date. The disease has characteristics of short stature, hip dislocation, minor vertebral and pelvic changes and microtia with hearing loss. There have been no further descriptions in the literature since 1981. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403617015 A rare primary bone defect, described only in a mother and her three daughters to date, characterized by short stature, hip dislocation, minor vertebral and pelvic changes, and microtia with hearing loss. There have been no further descriptions in the literature since 1981. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403618013 A rare primary bone defect, described only in a mother and her three daughters to date, characterised by short stature, hip dislocation, minor vertebral and pelvic changes, and microtia with hearing loss. There have been no further descriptions in the literature since 1981. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3416191001000116 Coxo-aurikuläres Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
962431000172115 syndrome coxo-auriculaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
962431000172115 syndrome coxo-auriculaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3416191001000116 Coxo-aurikuläres Syndrom 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
Coxoauricular syndrome (disorder) Is a Microtia true Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Is a Hearing loss associated with syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Is a Short stature disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Is a Multiple dislocations with dysplasia (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Coxoauricular syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Coxoauricular syndrome (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
Coxoauricular syndrome (disorder) Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Coxoauricular syndrome (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 4
Coxoauricular syndrome (disorder) Finding site External ear structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Coxoauricular syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Coxoauricular syndrome (disorder) Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Coxoauricular syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Coxoauricular syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Coxoauricular syndrome (disorder) Finding site External ear structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Coxoauricular syndrome (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Coxoauricular syndrome (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 1
Coxoauricular syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Coxoauricular syndrome (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 2
Coxoauricular syndrome (disorder) Associated morphology Dislocation true Inferred relationship Existential restriction modifier (core metadata concept) 3
Coxoauricular syndrome (disorder) Is a Chronic disease of ear (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Finding site Joint structure of multiple body sites (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Coxoauricular syndrome (disorder) Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Clinical course Progressive false Inferred relationship Existential restriction modifier (core metadata concept) 4
Coxoauricular syndrome (disorder) Interprets Hearing true Inferred relationship Existential restriction modifier (core metadata concept) 5
Coxoauricular syndrome (disorder) Is a Congenital anomaly of ear with impairment of hearing true Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Due to Spontaneous event (event) true Inferred relationship Existential restriction modifier (core metadata concept) 6
Coxoauricular syndrome (disorder) Is a Skeletal dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Is a Hip pathological dislocation (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Finding site Hip joint structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Coxoauricular syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Interprets Height / growth measure (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Coxoauricular syndrome (disorder) Associated morphology Damage false Inferred relationship Existential restriction modifier (core metadata concept) 7
Coxoauricular syndrome (disorder) Is a Injury of external ear (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Is a Bone injury true Inferred relationship Existential restriction modifier (core metadata concept)
Coxoauricular syndrome (disorder) Associated morphology Abnormal smallness (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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