{
    "disease_id": "DOID:0060879",
    "recommended_name": {
        "id": "DOID:0060879",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060879",
        "name": "primary hypomagnesemia",
        "description": "A metal metabolism disorder characterized by very low serum magnesium levels often with secondary hypocalcemia with onset typically in the first months of life."
    },
    "synonyms": [
        {
            "id": "DOID:0060879",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060879",
            "name": "HOMG",
            "description": ""
        },
        {
            "id": "DOID:0060879",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060879",
            "name": "primary familial hypomagnesemia",
            "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": "DOID:0060880",
            "label": "renal hypomagnesemia 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060881",
            "label": "renal hypomagnesemia 5 with ocular involvement",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060882",
            "label": "renal hypomagnesemia 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060883",
            "label": "intestinal hypomagnesemia 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060884",
            "label": "renal hypomagnesemia 6",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060885",
            "label": "renal hypomagnesemia 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060972",
            "label": "renal hypomagnesemia 7, with or without dilated cardiomyopathy",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0060883",
        "DOID:0060881",
        "DOID:0060879",
        "DOID:0060884",
        "DOID:0060972",
        "DOID:0060882",
        "DOID:0060880",
        "DOID:0060885"
    ],
    "unlinked_id_list": []
}