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

716999001: Joubert syndrome with renal defect (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3308138014 Joubert syndrome with renal defect (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308139018 Joubert syndrome with renal defect en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401442010 Joubert syndrome with renal defect is a rare subtype of Joubert syndrome and related disorders characterized by the neurological features of JS associated with renal disease, in the absence of retinopathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401443017 Joubert syndrome with renal defect is a rare subtype of Joubert syndrome and related disorders characterised by the neurological features of JS associated with renal disease, in the absence of retinopathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308138014 Joubert syndrome with renal defect (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308139018 Joubert syndrome with renal defect en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308140016 A rare subtype of Joubert syndrome with manifestation of the neurological features of Joubert Syndrome associated with renal disease, in the absence of retinopathy. Prevalence is unknown. In most cases the renal disease manifests as juvenile nephronophthisis, with onset of clinical symptoms in the late first/early second decade of life, although in rare cases there may be infantile nephronophthisis, with onset in the first years of life. The most commonly mutated genes in this subtype are NPHP1 (2q13) and RPGRIP1L (16q12.2) with autosomal recessive inheritance. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401442010 Joubert syndrome with renal defect is a rare subtype of Joubert syndrome and related disorders characterized by the neurological features of JS associated with renal disease, in the absence of retinopathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401443017 Joubert syndrome with renal defect is a rare subtype of Joubert syndrome and related disorders characterised by the neurological features of JS associated with renal disease, in the absence of retinopathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3385941001000111 Joubert-Syndrom mit Nierenstörung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
948401000172117 JS-R - Joubert syndrome with renal defect fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
961431000172110 syndrome de Joubert avec atteinte rénale fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
948401000172117 JS-R - Joubert syndrome with renal defect fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
961431000172110 syndrome de Joubert avec atteinte rénale fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3385941001000111 Joubert-Syndrom mit Nierenstörung 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
Joubert syndrome with renal defect Is a Joubert syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Joubert syndrome with renal defect Is a Hereditary nephropathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Joubert syndrome with renal defect Finding site Kidney structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Joubert syndrome with renal defect Associated morphology Aplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Joubert syndrome with renal defect Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Joubert syndrome with renal defect Finding site Cerebellar vermis structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Joubert syndrome with renal defect Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Joubert syndrome with renal defect Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Joubert syndrome with renal defect Associated morphology Aplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Joubert syndrome with renal defect Finding site Cerebellar vermis structure 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)

Back to Start