{
  "id": 13486,
  "label": "neonatal diabetes mellitus with congenital hypothyroidism",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012436",
  "properties": {
    "xrefs": [
      "DOID:0060638",
      "GARD:0016699",
      "MEDGEN:347541",
      "MESH:C565705",
      "OMIM:610199",
      "Orphanet:79118",
      "UMLS:C1857775"
    ],
    "synonyms": [
      "NDH syndrome",
      "neonatal diabetes mellitus with congenital hypothyroidism",
      "NDH",
      "Ndh syndrome",
      "diabetes mellitus, neonatal, with congenital hypothyroidism",
      "neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "A rare genetic disease characterized by intrauterine growth retardation, permanent neonatal diabetes mellitus, and congenital hypothyroidism. Additional manifestations include congenital glaucoma, hepatic disease (hepatitis, fibrosis, and cirrhosis), polycystic kidneys, exocrine pancreatic dysfunction, sensorineural hearing impairment, developmental delay, and mild facial dysmorphism (such as flat nasal bridge, epicanthal folds, long philtrum, and low-set ears), among others"
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16920,
      "label": "neonatal diabetes mellitus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16627
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11717",
          "GARD:0018682",
          "ICD10CM:P70.2",
          "ICD9:775.1",
          "MEDGEN:57645",
          "MedDRA:10028933",
          "NANDO:2200463",
          "NCIT:C99248",
          "Orphanet:224",
          "SCTID:49817004",
          "UMLS:C0158981",
          "icd11.foundation:1217915084"
        ],
        "synonyms": [
          "NDM",
          "congenital diabetes mellitus",
          "diabetes mellitus syndrome in newborn infant"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Neonatal diabetes mellitus presents as hyperglycemia, failure to thrive and, in some cases, dehydration and ketoacidosis which may be severe with coma, in a child within the first months of life."
      },
      "child_count": 4,
      "reference_id": "MONDO:0016391"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16920,
      "label": "neonatal diabetes mellitus"
    }
  ]
}