{
    "disease_id": "DOID:0060880",
    "recommended_name": {
        "id": "DOID:0060880",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060880",
        "name": "renal hypomagnesemia 3",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060880",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060880",
            "name": "familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement",
            "description": ""
        },
        {
            "id": "DOID:0060880",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060880",
            "name": "FHHNC without severe ocular involvement",
            "description": ""
        },
        {
            "id": "DOID:0060880",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060880",
            "name": "HOMG3",
            "description": ""
        },
        {
            "id": "DOID:0060880",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060880",
            "name": "isolated renal hypomagnesemia",
            "description": ""
        },
        {
            "id": "DOID:0060880",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060880",
            "name": "renal hypomagnesemia type 3",
            "description": ""
        },
        {
            "id": "DOID:0060880",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060880",
            "name": "primary hypomagnesemia due to defect in renal tubular transport of magnesium",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "renal hypomagnesemia 3",
            "description": "Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (FHHN) is a form of familial primary hypomagnesemia (FPH), characterized by recurrent urinary tract infections, nephrolithiasis, bilateral nephrocalcinosis, renal magnesium (Mg) wasting, hypercalciuria and kidney failure."
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "CLDN16 familial primary hypomagnesemia",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "CLDN16 primary hypomagnesemia",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "FHHNC without severe ocular involvement",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "HOMG3",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "familial primary hypomagnesemia caused by mutation in CLDN16",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "isolated renal hypomagnesemia",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "primary hypomagnesemia caused by mutation in CLDN16",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "primary hypomagnesemia due to defect in renal tubular transport of magnesium",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "renal hypomagnesemia type 3",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "hypercalciuria, childhood, self-limiting",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "hypomagnesemia 3, renal",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "hypomagnesemia, familial, with hypercalciuria and nephrocalcinosis",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "hypomagnesemia, familial, with hypercalciuria and nephrocalcinosis hypercalciuria, childhood, self-limiting, included",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "hypomagnesemia, isolated renal",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "hypomagnesemia, primary, due to defect in renal tubular Transport Of magnesium",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "hypomagnesemia, primary, due to defect in renal tubular Transport of magnesium",
            "description": ""
        },
        {
            "id": "MONDO:0009550",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009550",
            "name": "magnesium, defect in renal tubular transport of",
            "description": ""
        },
        {
            "id": "MIM:248250",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/248250",
            "name": "Hypomagnesemia 3",
            "description": "Hypomagnesemia 3"
        }
    ]
}