FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

716997004: Joubert syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3308127014 Joubert syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3308128016 Joubert syndrome en Synonym Active Case sensitive SNOMED CT core
3308129012 Congenital malformation of the brainstem and agenesis or hypoplasia of the cerebellar vermis leading to an abnormal respiratory pattern, nystagmus, hypotonia, ataxia, and delay in achieving motor milestones. Cognitive abilities are variable, ranging from severe intellectual deficit to normal intelligence. Careful examination of the face shows a characteristic appearance: large head, prominent forehead, high rounded eyebrow. The syndrome is genetically heterogeneous. Seven genes, AHI1 (6q23), NPHP1 (2q13), CEP290 (12q21), TMEM67 (8q22), RPGRIP1L (16q12), ARL13B (3p12.3-q12.3) and CC2D2A (4p15), and two loci on chromosomes 9q34 (JBTS1) and 11p12-q13 (CORS2/JBTS2) have been associated with the disease so far. Transmission is autosomal recessive. en Definition Active Case sensitive SNOMED CT core


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Joubert syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Joubert syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Joubert syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Joubert syndrome Is a Familial aplasia of the vermis true Inferred relationship Some
Joubert syndrome Is a Hereditary disorder of nervous system true Inferred relationship Some
Joubert syndrome Associated morphology Aplasia true Inferred relationship Some 1
Joubert syndrome Occurrence Congenital true Inferred relationship Some 1
Joubert syndrome Finding site Cerebellar vermis structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Joubert syndrome with ocular defect Is a True Joubert syndrome Inferred relationship Some
Joubert syndrome with renal defect Is a True Joubert syndrome Inferred relationship Some
Joubert syndrome with hepatic defect Is a True Joubert syndrome Inferred relationship Some
Joubert syndrome with oculorenal defect Is a True Joubert syndrome Inferred relationship Some
Joubert syndrome with orofaciodigital defect Is a True Joubert syndrome Inferred relationship Some
Joubert syndrome with Jeune asphyxiating thoracic dystrophy Is a True Joubert syndrome Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start