{
  "id": 13433,
  "label": "hyperinsulinemic hypoglycemia, familial, 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012382",
  "properties": {
    "xrefs": [
      "DOID:0070215",
      "GARD:0009870",
      "MEDGEN:400646",
      "MESH:C566493",
      "OMIM:609975",
      "Orphanet:71212",
      "SCTID:721236002",
      "UMLS:C1864948"
    ],
    "synonyms": [
      "HADH hyperinsulinemic hypoglycemia (disease)",
      "hyperinsulinemic hypoglycemia (disease) caused by mutation in HADH",
      "hyperinsulinemic hypoglycemia due to HADH deficiency",
      "hyperinsulinemic hypoglycemia due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency",
      "hyperinsulinemic hypoglycemia, familial, 4",
      "hyperinsulinemic hypoglycemia, familial, type 4",
      "hyperinsulinism due to SCHAD deficiency",
      "hyperinsulinism due to glutamodehydrogenase deficiency",
      "hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme a dehydrogenase deficiency",
      "hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency",
      "3-Alpha-hydroxyacyl-Coenzyme A dehydrogenase deficiency",
      "3-alpha hydroxyacyl-CoA dehydrogenase deficiency",
      "3-hydroxyacyl-CoA dehydrogenase deficiency",
      "3-hydroxyacyl-Coenzyme A dehydrogenase deficiency",
      "3-hydroxylacyl-CoA dehydrogenase deficiency",
      "HADH deficiency",
      "HADHSC deficiency",
      "HHF4",
      "L-3-Alpha-hydroxyacyl-CoA dehydrogenase, short chain, deficiency",
      "M-SCHAD deficiency",
      "M/SCHAD",
      "SCHAD deficiency",
      "SCHAD deficiency, formerly",
      "had deficiency",
      "medium and short chain 3-hydroxyacyl-CoA dehydrogenase deficiency"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Any hyperinsulinemic hypoglycemia in which the cause of the disease is a mutation in the HADH gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16411,
      "label": "diazoxide-sensitive diffuse hyperinsulinism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18925
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020067",
          "MEDGEN:1842739",
          "Orphanet:165985",
          "UMLS:C5679570"
        ],
        "synonyms": [
          "hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 8,
      "reference_id": "MONDO:0015624"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16411,
      "label": "diazoxide-sensitive diffuse hyperinsulinism"
    }
  ]
}