{
    "disease_id": "DOID:0060881", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009548", 
            "name": "familial hypomagnesemia with hypercalciuria, nephrocalcinosis and severe ocular involvement"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009548", 
            "name": "HOMG5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009548", 
            "name": "idiopathic hypercalciuria with bilateral macular colobomata"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009548", 
            "name": "FHHNC with severe ocular involvement"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009548", 
            "name": "bilateral macular coloboma with hypercalciuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009548", 
            "name": "hypomagnesemia, familial, with hypercalciuria, nephrocalcinosis, and severe ocular involvement"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009548", 
            "name": "familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009548", 
            "name": "hypomagnesemia 5, renal, with ocular involvement; HOMG5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009548", 
            "name": "hypercalciuria-bilateral macular coloboma syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009548", 
            "name": "hypomagnesemia, renal, with ocular involvement"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009548", 
            "name": "hypomagnesemia 5, renal, with ocular involvement"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009548", 
            "name": "Meier-Blumberg-Imahorn syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009548", 
            "name": "FHHNCOI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009548", 
            "name": "macular coloboma, bilateral, with hypercalciuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009548", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009548", 
            "name": "Meier Blumberg Imahorn syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060881", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060881", 
            "name": "FHHNC with severe ocular involvement"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060881", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060881", 
            "name": "Meier-Blumberg-Imahorn syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060881", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060881", 
            "name": "bilateral macular coloboma with hypercalciuria"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060881", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060881", 
            "name": "hypercalciuria-bilateral macular coloboma syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060881", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060881", 
            "name": "familial hypomagnesemia with hypercalciuria, nephrocalcinosis and severe ocular involvement"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060881", 
        "description": "A hypomagnesemia characterized by autosomal recessive inheritance of renal magnesium wasting with hypercalcinosis, progressive renal failure and severe ocular involvement that has material_basis_in homozygous mutation in the CLDN19 gene on chromosome 1p34.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060881", 
        "name": "renal hypomagnesemia 5 with ocular involvement"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060881#disease-associations", 
            "id": "0060881", 
            "database": "Alliance of Genome Resources"
        }
    ]
}