{
    "disease_id": "DOID:0080543", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009401", 
            "name": "ALDH4A1 hyperprolinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009401", 
            "name": "HPII"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009401", 
            "name": "1-pyrroline-5-carboxylate dehydrogenase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009401", 
            "name": "hyperprolinemia caused by mutation in ALDH4A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009401", 
            "name": "HYRPRO2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009401", 
            "name": "hyperprolinemia, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009401", 
            "name": "hyperprolinemia, type II; HYRPRO2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009401", 
            "name": "type 2 hyperprolinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009401", 
            "name": "1 alpha pyrroline-5-carboxylate dehydrogenase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009401", 
            "name": "hyperprolinemia, type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009401", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009401", 
            "name": "delta1-pyrroline-5-carboxylate dehydrogenase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080543", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080543", 
            "name": "hyperprolinemia type II"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080543", 
        "description": "A hyperprolinemia that has_material_basis_in homozygous or compound heterozygous mutation in the pyrroline-5-carboxylate dehydrogenase gene on chromosome 1p36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080543", 
        "name": "hyperprolinemia type 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080543#disease-associations", 
            "id": "0080543", 
            "database": "Alliance of Genome Resources"
        }
    ]
}