- OMIM ID
-
260565
- OMIM term:
- PEHO SYNDROME
- Alternative terms:
-
PROGRESSIVE ENCEPHALOPATHY WITH EDEMA, HYPSARRHYTHMIA, AND OPTIC ATROPHY
INFANTILE CEREBELLOOPTIC ATROPHY PEHO-LIKE SYNDROME, INCLUDED
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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