{
    "disease_id": "DOID:0060883",
    "recommended_name": {
        "id": "DOID:0060883",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060883",
        "name": "intestinal hypomagnesemia 1",
        "description": "A hypomagnesemia characterized by very low serum magnesium levels due to defects in intestinal absorption and kidney excretion and secondary hypocalcemia that has_material_basis_in homozygous or compound heterozygous mutations in the TRPM6 gene on chromosome 9q21."
    },
    "synonyms": [
        {
            "id": "DOID:0060883",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060883",
            "name": "HOMG1",
            "description": ""
        },
        {
            "id": "DOID:0060883",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060883",
            "name": "hypomagnesemia caused by selective magnesium malabsorption",
            "description": ""
        },
        {
            "id": "DOID:0060883",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060883",
            "name": "hypomagnesemia intestinal type 1",
            "description": ""
        },
        {
            "id": "DOID:0060883",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060883",
            "name": "hypomagnesemic tetany",
            "description": ""
        },
        {
            "id": "DOID:0060883",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060883",
            "name": "primary hypomagnesemia with secondary hypocalcemia",
            "description": ""
        },
        {
            "id": "DOID:0060883",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060883",
            "name": "intestinal hypomagnesemia with secondary hypocalcemia",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "intestinal hypomagnesemia 1",
            "description": "Primary hypomagnesemia with secondary hypocalcemia (PHSH) is a form of familial primary hypomagnesemia (FPH), characterized by severe hypomagnesemia and secondary hypocalcemia associated with neurological symptoms, including generalized seizures, tetany and muscle spasms. PHSH may be fatal or may result in chronic irreversible neurological complications."
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "HOMG1",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "HSH",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "PHSH",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "TRPM6 familial primary hypomagnesemia",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "TRPM6 primary hypomagnesemia",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "familial primary hypomagnesemia caused by mutation in TRPM6",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "hypomagnesemia caused by selective magnesium malabsorption",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "hypomagnesemia intestinal type 1",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "hypomagnesemic tetany",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "intestinal hypomagnesemia type 1",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "intestinal hypomagnesemia with secondary hypocalcemia",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "primary hypomagnesemia caused by mutation in TRPM6",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "primary hypomagnesemia with secondary hypocalcemia",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "hypomagnesemia 1, intestinal",
            "description": ""
        },
        {
            "id": "MIM:602014",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/602014",
            "name": "Hypomagnesemia 1",
            "description": "Hypomagnesemia 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060883"
    ],
    "unlinked_id_list": []
}