{
    "disease_id": "DOID:0060882", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012717", 
            "name": "hypomagnesemia 4, renal; HOMG4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012717", 
            "name": "familial primary hypomagnesemia caused by mutation in EGF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012717", 
            "name": "primary hypomagnesemia caused by mutation in EGF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012717", 
            "name": "hypomagnesemia, renal, Normocalciuric"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012717", 
            "name": "renal hypomagnesemia type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012717", 
            "name": "EGF primary hypomagnesemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012717", 
            "name": "EGF familial primary hypomagnesemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012717", 
            "name": "hypomagnesemia 4, renal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012717", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012717", 
            "name": "HOMG4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060882", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060882", 
            "name": "HOMG4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060882", 
        "description": "A hypomagnesemia characterized by isolated hypomagnesemia due to renal loss with normal serum calcium levels and urinary calcium excretion that has material_basis_in variation in the chromosome region 4q25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060882", 
        "name": "renal hypomagnesemia 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060882#disease-associations", 
            "id": "0060882", 
            "database": "Alliance of Genome Resources"
        }
    ]
}