{
    "disease_id": "DOID:0110914", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009427", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009427", 
            "name": "HOPS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009427", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009427", 
            "name": "hypophosphatasia, perinatal lethal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009427", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009427", 
            "name": "phosphoethanolaminuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009427", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009427", 
            "name": "hypophosphatasia, infantile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009427", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009427", 
            "name": "infantile Rathburn disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009427", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009427", 
            "name": "infantile phosphoethanolaminuria"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110914", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110914", 
            "name": "Hops"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110914", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110914", 
            "name": "phosphoethanolaminuria"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110914", 
        "description": "A hypophosphatasia that has_material_basis_in homozygous or compound heterozygosity mutation in the gene encoding tissue-nonspecific alkaline phosphatase (ALPL) on chromosome 1p36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110914", 
        "name": "infantile hypophosphatasia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110914#disease-associations", 
            "id": "0110914", 
            "database": "Alliance of Genome Resources"
        }
    ]
}