{
    "disease_id": "DOID:0090109", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011013", 
            "name": "autosomal dominant hypocalcemia 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011013", 
            "name": "hypocalcemia, autosomal dominant 1; HYPOC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011013", 
            "name": "CASR autosomal dominant hypocalcemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011013", 
            "name": "HYPOC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011013", 
            "name": "autosomal dominant hypocalcemia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011013", 
            "name": "hypocalcemia, autosomal dominant 1, with Bartter syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011013", 
            "name": "hypocalcemia, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011013", 
            "name": "hypocalcemia, autosomal dominant type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011013", 
            "name": "hypocalcemia, autosomal dominant 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011013", 
            "name": "autosomal dominant hypocalcemia caused by mutation in CASR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011013", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011013", 
            "name": "hypercalciuric hypocalcemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090109", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090109", 
            "name": "HYPOC"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090109", 
        "description": "A metal metabolism disorder characterized by autosomal dominant inheritance of variable degrees of hypocalcemia with normal to low levels of parathyroid hormone.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090109", 
        "name": "autosomal dominant hypocalcemia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090109#disease-associations", 
            "id": "0090109", 
            "database": "Alliance of Genome Resources"
        }
    ]
}