{
    "disease_id": "DOID:0060882",
    "recommended_name": {
        "id": "DOID:0060882",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060882",
        "name": "renal hypomagnesemia 4",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060882",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060882",
            "name": "HOMG4",
            "description": ""
        },
        {
            "id": "MONDO:0012717",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012717",
            "name": "renal hypomagnesemia 4",
            "description": "Any primary hypomagnesemia in which the cause of the disease is a mutation in the EGF gene."
        },
        {
            "id": "MONDO:0012717",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012717",
            "name": "hypomagnesemia 4, renal; HOMG4",
            "description": ""
        },
        {
            "id": "MONDO:0012717",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012717",
            "name": "familial primary hypomagnesemia caused by mutation in EGF",
            "description": ""
        },
        {
            "id": "MONDO:0012717",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012717",
            "name": "primary hypomagnesemia caused by mutation in EGF",
            "description": ""
        },
        {
            "id": "MONDO:0012717",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012717",
            "name": "hypomagnesemia, renal, Normocalciuric",
            "description": ""
        },
        {
            "id": "MONDO:0012717",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012717",
            "name": "renal hypomagnesemia type 4",
            "description": ""
        },
        {
            "id": "MONDO:0012717",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012717",
            "name": "EGF primary hypomagnesemia",
            "description": ""
        },
        {
            "id": "MONDO:0012717",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012717",
            "name": "EGF familial primary hypomagnesemia",
            "description": ""
        },
        {
            "id": "MONDO:0012717",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012717",
            "name": "hypomagnesemia 4, renal",
            "description": ""
        },
        {
            "id": "MONDO:0012717",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012717",
            "name": "HOMG4",
            "description": ""
        },
        {
            "id": "MIM:611718",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/611718",
            "name": "Hypomagnesemia 4",
            "description": "Hypomagnesemia 4"
        }
    ]
}