{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009504", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009504", 
            "name": "mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009504", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009504", 
            "name": "lactic acidosis, fatal infantile, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009504", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009504", 
            "name": "MTDPS9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009504", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009504", 
            "name": "lactic acidosis, fatal infantile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009504", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009504", 
            "name": "lactic acidosis congenital infantile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009504", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009504", 
            "name": "mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria); MTDPS9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009504", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009504", 
            "name": "mitochondrial DNA depletion syndrome type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009504", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009504", 
            "name": "SUCLG1 mitochondrial DNA depletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009504", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009504", 
            "name": "mitochondrial DNA depletion syndrome caused by mutation in SUCLG1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009504", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009504", 
            "name": "fatal infantile lactic acidosis with methylmalonic aciduria"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080128", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080128", 
            "name": "fatal infantile lactic acidosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080128", 
        "description": "A mitochondrial DNA depletion syndrome that is characterized by infantile onset of hypotonia, lactic acidosis, severe psychomotor retardation, progressive neurologic deterioration, and excretion of methylmalonic acid, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the alpha subunit of the succinate-CoA ligase gene on chromosome 2p11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080128", 
        "name": "mitochondrial DNA depletion syndrome 9"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/245400", 
            "id": "245400", 
            "database": "MIM"
        }
    ]
}