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ONTOLOGY REPORT - ANNOTATIONS


Term:PEHO Syndrome
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Accession:DOID:9003922 term browser browse the term
Synonyms:exact_synonym: Infantile cerebellooptic atrophy;   PEHO;   PEHO-Like Syndrome;   Progressive Encephalopathy with edema, Hypsarrhythmia, and Optic atrophy
 primary_id: MESH:C536317;   RDO:0001850
 alt_id: OMIM:260565
For additional species annotation, visit the Alliance of Genome Resources.


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PEHO Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ccdc88a coiled coil domain containing 88A JBrowse link 14 113,771,093 113,936,376 RGD:11554173
RGD:8554872
G Igf1 insulin-like growth factor 1 JBrowse link 7 28,412,123 28,491,815 RGD:8548849
G Kif1a kinesin family member 1A JBrowse link 9 100,171,851 100,253,626 RGD:8554872
G Znhit3 zinc finger, HIT-type containing 3 JBrowse link 10 72,227,710 72,235,932 RGD:8554872
RGD:11554173

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14025
    syndrome 4467
      PEHO Syndrome 4
Path 2
Term Annotations click to browse term
  disease 14025
    disease of anatomical entity 13238
      nervous system disease 8245
        central nervous system disease 5483
          brain disease 5121
            epilepsy 891
              electroclinical syndrome 230
                infancy electroclinical syndrome 108
                  West syndrome 108
                    PEHO Syndrome 4
paths to the root