{
    "disease_id": "DOID:0060880", 
    "synonyms": [
        {
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            "description": "", 
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        {
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            "description": "", 
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        {
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            "description": "", 
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        {
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            "description": "", 
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        {
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            "description": "", 
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        {
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            "description": "", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
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        }, 
        {
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            "description": "", 
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            "id": "MONDO:0009550", 
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009550", 
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            "description": "", 
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        }, 
        {
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            "description": "", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009550", 
            "description": "", 
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009550", 
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        }, 
        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
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        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009550", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009550", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009550", 
            "name": "hypomagnesemia 3, renal"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060880", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060880", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060880", 
            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "FHHNC without severe ocular involvement"
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        {
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            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "HOMG3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060880", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060880", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060880", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060880", 
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        }, 
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060880", 
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        }, 
        {
            "url": "https://www.omim.org/entry/248250", 
            "description": "", 
            "resource": "MIM", 
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            "name": "Hypomagnesemia 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060880", 
        "description": "A hypomagnesemia characterized by autosomal recessive inheritance of excessive urinary Ca(2+) and Mg(2+) excretion that has material_basis_in homozygous or compound heterozygous mutation in the CLDN16 gene on chromosome 3q28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060880", 
        "name": "renal hypomagnesemia 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/248250", 
            "id": "248250", 
            "database": "MIM"
        }
    ]
}