Send us a Message

Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   


RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:Mitchell syndrome
go back to main search page
Accession:DOID:0070516 term browser browse the term
Definition:A peroxisomal disease characterized by progressive episodic demyelination, sensorimotor polyneuropathy, and hearing loss that has_material_basis_in heterozygous mutation in the ACOX1 gene on chromosome 17q25.1. (DO)
Synonyms:exact_synonym: MITCH
 primary_id: MIM:618960
 alt_id: DOID:9002088
 xref: ORDO:631248

show annotations for term's descendants           Sort by:
Mitchell syndrome term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Acox1 acyl-CoA oxidase 1 ISO ClinVar Annotator: match by term: Mitchell syndrome OMIM
PMID:8040306 PMID:16199547 PMID:17458872 PMID:25741868 PMID:28492532 More... NCBI chr10:101,406,197...101,431,252
Ensembl chr10:101,406,197...101,431,232
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19072
    sensory system disease 7197
      Hearing Disorders 829
        Hearing Loss 824
          Mitchell syndrome 1
Path 2
Term Annotations click to browse term
  disease 19072
    disease of anatomical entity 18365
      nervous system disease 14222
        Neurologic Manifestations 10288
          sensory system disease 7197
            Otorhinolaryngologic Diseases 1781
              auditory system disease 1040
                Hearing Disorders 829
                  Hearing Loss 824
                    Mitchell syndrome 1
paths to the root