Human Disease Ontology

Last uploaded: November 1, 2024
Preferred Name

Joubert syndrome
Synonyms

JBTS

Definitions

A ciliopathy that is 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. Xref MGI.

ID

http://purl.obolibrary.org/obo/DOID_0050777

comment

Xref MGI.

created_by

lschriml

creation_date

2013-04-04T11:25:32Z

database_cross_reference

MIM:PS213300

ICD10CM:Q04.3

GARD:6802

ORDO:475

definition

A ciliopathy that is 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.

disease has location

http://purl.obolibrary.org/obo/UBERON_0000955

has exact synonym

JBTS

has_obo_namespace

disease_ontology

id

DOID:0050777

in_subset

http://purl.obolibrary.org/obo/doid#DO_rare_slim

label

Joubert syndrome

notation

DOID:0050777

prefLabel

Joubert syndrome

subClassOf

http://purl.obolibrary.org/obo/DOID_0060340

http://purl.obolibrary.org/obo/DOID_936

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_0050777 DTO SAME_URI
http://purl.obolibrary.org/obo/DOID_0050777 HHEAR SAME_URI
http://purl.obolibrary.org/obo/DOID_0050777 DDSS SAME_URI
http://purl.obolibrary.org/obo/DOID_0050777 NIFSTD SAME_URI
http://purl.obolibrary.org/obo/DOID_0050777 FNS-H SAME_URI
http://purl.obolibrary.org/obo/MONDO_0018772 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0018772 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0018772 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0018772 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0018772 DOVES LOOM
http://purl.obolibrary.org/obo/MONDO_0018772 KTAO LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0431399 OCHV LOOM
http://purl.bioontology.org/ontology/MEDDRA/10078574 MEDDRA LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Joubert_Syndrome CSEO LOOM
http://purl.obolibrary.org/obo/OMIM_213300 CCO LOOM
http://purl.obolibrary.org/obo/DOID_0050777 DTO LOOM
http://purl.obolibrary.org/obo/DOID_0050777 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_0050777 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_0050777 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_0050777 FNS-H LOOM
http://www.orpha.net/ORDO/Orphanet_475 ORDO LOOM
http://purl.obolibrary.org/obo/NCIT_C74996 BERO LOOM
rgo:16657 GAMUTS LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C74996 NCIT LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/716997004 SNOMEDCT LOOM
http://www.limics.org/hrdo/rdfns#pat_id_1022 HRDO LOOM
http://purl.jp/bio/4/id/200906090111191439 IOBC LOOM
http://www.gamuts.net/entity#Joubert_syndrome GAMUTS REST