{
    "disease_id": "DOID:0110853", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010823", 
            "name": "RCDP3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010823", 
            "name": "rhizomelic chondrodysplasia punctata, type 3; RCDP3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010823", 
            "name": "Alkyglycerone-phosphate synthase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010823", 
            "name": "AGPS rhizomelic chondrodysplasia punctata"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010823", 
            "name": "alkylglycerone-phosphate synthase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010823", 
            "name": "Agps deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010823", 
            "name": "alkyldihydroxyacetonephosphate synthase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010823", 
            "name": "rhizomelic chondrodysplasia punctata, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010823", 
            "name": "rhizomelic chondrodysplasia punctata caused by mutation in AGPS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110853", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110853", 
            "name": "Agps Deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110853", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110853", 
            "name": "Alkyldihydroxyacetonephosphate Synthase Deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110853", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110853", 
            "name": "Alkylglycerone-Phosphate Synthase Deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110853", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110853", 
            "name": "Rcdp3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110853", 
        "description": "A rhizomelic chondrodysplasia punctata that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the AGPS gene on chromosome 2q31.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110853", 
        "name": "rhizomelic chondrodysplasia punctata type 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110853#disease-associations", 
            "id": "0110853", 
            "database": "Alliance of Genome Resources"
        }
    ]
}