{
    "disease_id": "DOID:0060885",
    "recommended_name": {
        "id": "DOID:0060885",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060885",
        "name": "renal hypomagnesemia 2",
        "description": "A hypomagnesemia characterized by autosomal dominant inheritance of hypomagnesemia due to renal magnesium loss that has_material_basis_in heterozygous mutation in the FXYD2 gene on chromosome 11q23."
    },
    "synonyms": [
        {
            "id": "DOID:0060885",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060885",
            "name": "HOMG2",
            "description": ""
        },
        {
            "id": "DOID:0060885",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060885",
            "name": "autosomal dominant primary hypomagnesemia with hypocalciuria",
            "description": ""
        },
        {
            "id": "MONDO:0007937",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007937",
            "name": "renal hypomagnesemia 2",
            "description": "Autosomal dominant primary hypomagnesemia with hypocalciuria (ADPHH) is a mild form of familial primary hypomagnesemia (FPH), characterized by extreme weakness, tetany and convulsions. Secondary disturbances in calcium excretion are observed."
        },
        {
            "id": "MONDO:0007937",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007937",
            "name": "FXYD2 familial primary hypomagnesemia",
            "description": ""
        },
        {
            "id": "MONDO:0007937",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007937",
            "name": "FXYD2 primary hypomagnesemia",
            "description": ""
        },
        {
            "id": "MONDO:0007937",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007937",
            "name": "HOMG2",
            "description": ""
        },
        {
            "id": "MONDO:0007937",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007937",
            "name": "familial primary hypomagnesemia caused by mutation in FXYD2",
            "description": ""
        },
        {
            "id": "MONDO:0007937",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007937",
            "name": "isolated autosomal dominant hypomagnesemia",
            "description": ""
        },
        {
            "id": "MONDO:0007937",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007937",
            "name": "isolated renal magnesium wasting",
            "description": ""
        },
        {
            "id": "MONDO:0007937",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007937",
            "name": "primary hypomagnesemia caused by mutation in FXYD2",
            "description": ""
        },
        {
            "id": "MONDO:0007937",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007937",
            "name": "renal hypomagnesemia type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007937",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007937",
            "name": "hypomagnesemia 2, renal",
            "description": ""
        },
        {
            "id": "MIM:154020",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/154020",
            "name": "Hypomagnesemia 2",
            "description": "Hypomagnesemia 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060885"
    ],
    "unlinked_id_list": []
}