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
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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: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

Term paths to the root
Path 1
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  disease 14875
    syndrome 4220
      PEHO Syndrome 4
Path 2
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  disease 14875
    disease of anatomical entity 14051
      nervous system disease 9116
        central nervous system disease 6913
          brain disease 6418
            epilepsy 1017
              electroclinical syndrome 282
                infancy electroclinical syndrome 152
                  West syndrome 152
                    PEHO Syndrome 4
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.