{
  "id": 15627,
  "label": "hypomagnesemia, seizures, and intellectual disability",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014631",
  "properties": {
    "xrefs": [
      "GARD:0025007",
      "OMIMPS:616418"
    ],
    "synonyms": [
      "hypomagnesemia, seizures, and intellectual disability",
      "hypomagnesemia, seizures, and mental retardation",
      "HOMGSMR"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 18260,
      "label": "familial primary hypomagnesemia with normocalciuria and normocalcemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17903
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025127",
          "MEDGEN:1390277",
          "Orphanet:34527",
          "SCTID:725031005",
          "UMLS:C4510731"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "Familial primary hypomagnesemia with normocalciuria and normocalcemia (FPHNN) is a form of familial primary hypomagnesemia (FPH), characterized by low serum magnesium (Mg) values but inappropriate normal urinary Mg values (i.e. renal hypomagnesemia). The typical symptoms are weakness of the limbs, vertigo, headaches, seizures, brisk tendon reflexes and mild to moderate psychomotor delay."
      },
      "child_count": 3,
      "reference_id": "MONDO:0018101"
    }
  ],
  "children": [
    {
      "id": 20186,
      "label": "hypomagnesemia, seizures, and intellectual disability 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        15627
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025248",
          "MEDGEN:906582",
          "OMIM:616418",
          "UMLS:C4225333"
        ],
        "synonyms": [
          "hypomagnesemia, seizures, and mental retardation",
          "HOMGSMR1",
          "HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020787"
    },
    {
      "id": 20187,
      "label": "hypomagnesemia, seizures, and intellectual disability 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        15627
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025249",
          "MEDGEN:1675904",
          "OMIM:618314",
          "UMLS:C5193023"
        ],
        "synonyms": [
          "HOMGSMR2",
          "HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020788"
    }
  ],
  "roots": [
    {
      "id": 18260,
      "label": "familial primary hypomagnesemia with normocalciuria and normocalcemia"
    }
  ]
}