{
    "disease_id": "DOID:0080539",
    "recommended_name": {
        "id": "DOID:0080539",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080539",
        "name": "PEHO syndrome",
        "description": "A brain disease that is characterized by extreme cerebellar atrophy due to almost total granule neuron loss."
    },
    "synonyms": [
        {
            "id": "MONDO:0009841",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009841",
            "name": "PEHO syndrome",
            "description": "PEHO (Progressive encephalopathy with Edema, Hypsarrhythmia and Optic atrophy) syndrome is a rare neurodegenerative disorder belonging to the group of infantile progressive encephalopathies."
        },
        {
            "id": "MONDO:0009841",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009841",
            "name": "peho syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009841",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009841",
            "name": "progressive encephalopathy with edema, hypsarrhythmia and optic atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009841",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009841",
            "name": "progressive encephalopathy-optic atrophy syndrome",
            "description": ""
        },
        {
            "id": "MIM:260565",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/260565",
            "name": "PEHO syndrome",
            "description": "PEHO syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080539"
    ],
    "unlinked_id_list": []
}