{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "Alpers-Huttenlocher syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "Alpers Huttenlocher syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "mitochondrial DNA depletion syndrome 4A (Alpers type)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "Poliodystrophia cerebri progressiva"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "Alpers progressive infantile poliodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "Alpers Huttenlocher disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "infantile poliodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "progressive sclerosing poliodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "diffuse cerebral degeneration in infancy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "Alpers diffuse Degeneration of cerebral Gray matter with hepatic cirrhosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "PNDC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "Alpers progressive sclerosing poliodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "Alpers syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "MTDPS4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "Alper's syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "Alpers' disease or gray-matter degeneration"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "mitochondrial DNA depletion syndrome type 4a"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "mitochondrial DNA depletion syndrome 4A (Alpers type); MTDPS4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "progressive neuronal degeneration of childhood with liver disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "Alper syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "neuronal Degeneration of childhood with liver disease, progressive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "AHD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "Alpers disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "AHS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008758", 
            "name": "progressive cerebral poliodystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080122", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080122", 
            "name": "Alper's syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080122", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080122", 
            "name": "Alpers disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080122", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080122", 
            "name": "Alpers progressive infantile poliodystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080122", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080122", 
            "name": "Alpers syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080122", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080122", 
            "name": "Alpers' disease or gray-matter degeneration"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080122", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080122", 
            "name": "Alpers-Huttenlocher syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080122", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080122", 
            "name": "progressive sclerosing poliodystrophy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080122", 
        "description": "A mitochondrial DNA depletion syndrome that is characterized by a clinical triad of psychomotor retardation, intractable epilepsy, and liver failure in infants and young children, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the nuclear gene encoding mitochondrial DNA polymerase gamma on chromosome 15q26.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080122", 
        "name": "mitochondrial DNA depletion syndrome 4a"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/203700", 
            "id": "203700", 
            "database": "MIM"
        }
    ]
}