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

733418003: Joubert syndrome with Jeune asphyxiating thoracic dystrophy (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
3499398014 Joubert syndrome with JATD (Jeune asphyxiating thoracic dystrophy) en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3499399018 Joubert syndrome with Jeune asphyxiating thoracic dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3499400013 Joubert syndrome with Jeune asphyxiating thoracic dystrophy (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403773019 A rare genetic developmental defect during embryogenesis characterized by the association of the classic features of Joubert syndrome (congenital midbrain-hindbrain malformations causing hypotonia, abnormal breathing and eye movements, ataxia and cognitive impairment) together with the skeletal anomalies of Jeune asphyxiating thoracic dystrophy (short ribs, long and narrow thorax causing respiratory failure, short-limbs, short stature, and polydactyly). Additional variable manifestations include cystic kidneys, liver fibrosis, and retinal dystrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403774013 A rare genetic developmental defect during embryogenesis characterised by the association of the classic features of Joubert syndrome (congenital midbrain-hindbrain malformations causing hypotonia, abnormal breathing and eye movements, ataxia and cognitive impairment) together with the skeletal anomalies of Jeune asphyxiating thoracic dystrophy (short ribs, long and narrow thorax causing respiratory failure, short-limbs, short stature, and polydactyly). Additional variable manifestations include cystic kidneys, liver fibrosis, and retinal dystrophy. 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
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Is a Jeune thoracic dystrophy (disorder) true Inferred relationship Some
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Is a Joubert syndrome (disorder) true Inferred relationship Some
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Occurrence Congenital false Inferred relationship Some 4
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Occurrence Congenital false Inferred relationship Some 5
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Associated morphology Aplasia false Inferred relationship Some 6
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Occurrence Congenital false Inferred relationship Some 6
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Finding site Cerebellar vermis structure false Inferred relationship Some 6
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Associated morphology Abnormally short growth false Inferred relationship Some 4
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Finding site Entire limb false Inferred relationship Some 4
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Associated morphology Congenital dysplasia false Inferred relationship Some 5
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Finding site Bone structure of rib false Inferred relationship Some 5
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Occurrence Congenital true Inferred relationship Some 1
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Associated morphology Aplasia true Inferred relationship Some 2
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Finding site Cerebellar vermis structure true Inferred relationship Some 2
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Occurrence Congenital true Inferred relationship Some 3
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Occurrence Congenital true Inferred relationship Some 2
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Associated morphology Abnormally short growth true Inferred relationship Some 1
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Associated morphology Congenital dysplasia false Inferred relationship Some 3
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Finding site Bone structure of rib true Inferred relationship Some 3
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Finding site Entire limb true Inferred relationship Some 1
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Associated morphology Dysplasia true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

Back to Start