{
  "id": 9267,
  "label": "renal hypomagnesemia 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007937",
  "properties": {
    "xrefs": [
      "DOID:0060885",
      "GARD:0003350",
      "MEDGEN:320542",
      "MESH:C537152",
      "OMIM:154020",
      "Orphanet:34528",
      "SCTID:725393000",
      "UMLS:C1835171"
    ],
    "synonyms": [
      "FXYD2 familial primary hypomagnesemia",
      "FXYD2 primary hypomagnesemia",
      "HOMG2",
      "familial primary hypomagnesemia caused by mutation in FXYD2",
      "isolated autosomal dominant hypomagnesemia",
      "isolated renal magnesium wasting",
      "primary hypomagnesemia caused by mutation in FXYD2",
      "renal hypomagnesemia type 2",
      "autosomal dominant primary hypomagnesemia with hypocalciuria",
      "hypomagnesemia 2, renal",
      "magnesium loss, isolated renal",
      "magnesium wasting, renal"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17902,
      "label": "familial primary hypomagnesemia with hypocalcuria",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18259
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025120",
          "Orphanet:306519",
          "SCTID:711151004"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 1,
      "reference_id": "MONDO:0017625"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17902,
      "label": "familial primary hypomagnesemia with hypocalcuria"
    }
  ]
}