A rare subtype of Joubert syndrome and related disorders (JSRD) characterized by the neurological features of JS associated with renal disease, in the absence of retinopathy. [ Orphanet:220497 ]
Synonyms: Joubert syndrome type 4 JS-R JBTS4
Term information
- MEDGEN:335526 (MONDO:equivalentTo)
- UMLS:C1846790 (MONDO:equivalentTo)
- OMIM:609583 (Orphanet:220497/e)
- SCTID:716999001 (MONDO:equivalentTo)
- DOID:0110999 (MONDO:equivalentTo)
- MESH:C536296 (MONDO:equivalentTo)
- NCIT:C74997 (MONDO:equivalentTo)
- GARD:10169 (MONDO:GARD)
- Orphanet:220497 (OMIM:609583)
gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare
http://www.orpha.net/ORDO/Orphanet_220497
http://purl.obolibrary.org/obo/DOID_0110999
https://omim.org/entry/609583
http://purl.obolibrary.org/obo/NCIT_C74997
http://identifiers.org/snomedct/716999001
http://identifiers.org/mesh/C536296
http://identifiers.org/medgen/335526
http://linkedlifedata.com/resource/umls/id/C1846790
http://purl.obolibrary.org/obo/MONDO_0019741
http://purl.obolibrary.org/obo/MONDO_0020022