{
    "disease_id": "DOID:0060883",
    "recommended_name": {
        "id": "DOID:0060883",
        "resource": "Disease Ontology",
        "url": "http://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 absorbtion 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": "http://disease-ontology.org/term/DOID:0060883",
            "name": "HOMG1",
            "description": ""
        },
        {
            "id": "DOID:0060883",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060883",
            "name": "hypomagnesemia caused by selective magnesium malabsorption",
            "description": ""
        },
        {
            "id": "DOID:0060883",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060883",
            "name": "hypomagnesemia intestinal type 1",
            "description": ""
        },
        {
            "id": "DOID:0060883",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060883",
            "name": "hypomagnesemic tetany",
            "description": ""
        },
        {
            "id": "DOID:0060883",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060883",
            "name": "primary hypomagnesemia with secondary hypocalcemia",
            "description": ""
        },
        {
            "id": "DOID:0060883",
            "resource": "Disease Ontology",
            "url": "http://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, see this term), 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": "hypomagnesemia caused by selective magnesium malabsorption",
            "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": "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": "hypomagnesemia intestinal 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": "hypomagnesemia 1, intestinal; HOMG1",
            "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": "intestinal hypomagnesemia type 1",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "hypomagnesemia with secondary hypocalcemia",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "hypomagnesemia, intestinal, with secondary hypocalcemia",
            "description": ""
        },
        {
            "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": "familial primary hypomagnesemia caused by mutation in TRPM6",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "Homg",
            "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": "primary hypomagnesemia caused by mutation in TRPM6",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "hypomagnesemia 1, intestinal",
            "description": ""
        },
        {
            "id": "MONDO:0011176",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011176",
            "name": "TRPM6 primary hypomagnesemia",
            "description": ""
        },
        {
            "id": "MIM:602014",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/602014",
            "name": "Hypomagnesemia 1",
            "description": "Hypomagnesemia 1"
        }
    ]
}