has material basis in germline mutation in ZNHIT3 syndromic disease PEHO syndrome https://github.com/monarch-initiative/mondo/issues/6878 https://rarediseases.info.nih.gov/diseases/4264/peho-syndrome https://www.malacards.org/card/peho_syndrome infantile Cerebellooptic atrophy MONDO:0009841 MEDGEN:342404 DOID:0080539 OMIM:260565 progressive encephalopathy-optic atrophy syndrome peho-like syndrome PEHO (Progressive encephalopathy with Edema, Hypsarrhythmia and Optic atrophy) syndrome is a rare neurodegenerative disorder belonging to the group of infantile progressive encephalopathies. MESH:C536317 GARD:0004264 UMLS:C1850055 Orphanet:2836 icd11.foundation:976613527 peho syndrome progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy peho progressive encephalopathy with edema, hypsarrhythmia and optic atrophy epilepsy syndrome inherited neurodegenerative disorder