Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024
Preferred Name

Joubert syndrome
Synonyms

Joubert syndrome type A

Joubert-Boltshauser syndrome

CPD IV

Cerebelloparenchymal disorder IV

Pure Joubert syndrome

Classic Joubert syndrome

Definitions

A rare, autosomal recessive congenital cerebellar ataxia characterized by 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.

ID

http://www.orpha.net/ORDO/Orphanet_475

alternative_term

Joubert syndrome type A

Joubert-Boltshauser syndrome

CPD IV

Cerebelloparenchymal disorder IV

Pure Joubert syndrome

Classic Joubert syndrome

definition

A rare, autosomal recessive congenital cerebellar ataxia characterized by 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.

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=475

has_age_of_onset

Antenatal

has_inheritance

Autosomal recessive

hasDbXref

ICD-11:LD20.00

OMIM:300804

OMIM:608091

OMIM:615665

OMIM:619476

OMIM:615636

OMIM:619582

OMIM:618161

OMIM:614424

OMIM:619562

OMIM:213300

OMIM:617622

OMIM:614173

OMIM:616784

OMIM:616781

ICD-10:Q04.3

UMLS:C0431399

OMIM:618763

OMIM:610188

OMIM:612291

OMIM:616654

OMIM:614615

OMIM:614464

OMIM:614465

OMIM:608629

OMIM:609583

OMIM:614815

OMIM:619185

OMIM:612285

OMIM:610688

OMIM:617121

OMIM:617120

MedDRA:10078574

OMIM:617757

OMIM:617767

OMIM:617761

OMIM:611560

OMIM:614970

OMIM:616490

label

Joubert syndrome

notation

ORPHA:475

part_of

http://www.orpha.net/ORDO/Orphanet_269560

http://www.orpha.net/ORDO/Orphanet_98514

http://www.orpha.net/ORDO/Orphanet_611327

http://www.orpha.net/ORDO/Orphanet_102283

http://www.orpha.net/ORDO/Orphanet_140874

prefixIRI

ORDO:Orphanet_475

prefLabel

Joubert syndrome

present_in

Italy AND has_point_prevalence_average_value : 0.47 AND has_point_prevalence_range : 1-9 / 1 000 000

Worldwide AND has_birth_prevalence_average_value : 1.6666 AND has_birth_prevalence_range : 1-9 / 100 000

Spain AND has_birth_prevalence_average_value : 5.0 AND has_birth_prevalence_range : 1-9 / 100 000

Worldwide AND has_point_prevalence_range : Unknown

treeView

http://www.orpha.net/ORDO/Orphanet_269560

http://www.orpha.net/ORDO/Orphanet_98514

http://www.orpha.net/ORDO/Orphanet_611327

http://www.orpha.net/ORDO/Orphanet_102283

http://www.orpha.net/ORDO/Orphanet_140874

subClassOf

http://www.orpha.net/ORDO/Orphanet_377789

http://www.orpha.net/ORDO/Orphanet_557493

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