{
  "id": 13390,
  "label": "obesity due to pro-opiomelanocortin deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012335",
  "properties": {
    "xrefs": [
      "GARD:0010823",
      "ICD9:255.5",
      "MEDGEN:341863",
      "MESH:C565726",
      "NORD:110450",
      "OMIM:609734",
      "Orphanet:71526",
      "SCTID:702949005",
      "UMLS:C1857854",
      "icd11.foundation:530374033"
    ],
    "synonyms": [
      "POMC Deficiency",
      "POMC deficiency",
      "obesity, adrenal insufficiency, and red hair due to POMC deficiency",
      "OBAIRH",
      "PROOPIOMELANOCORTIN deficiency",
      "obesity, early-onset, adrenal insufficiency, and Red hair",
      "obesity, early-onset, with adrenal insufficiency and RED hair",
      "obesity, early-onset, with adrenal insufficiency and Red hair"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Pro-opiomelanocortin (POMC) deficiency is a form of monogenic obesity resulting in severe early-onset obesity, adrenal insufficiency, red hair and pale skin."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19055,
      "label": "inherited obesity",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6875,
        12246
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018935",
          "MEDGEN:885912",
          "OMIM:601665",
          "Orphanet:77828",
          "UMLS:C4054476"
        ],
        "synonyms": [
          "genetic obesity",
          "genetic obesity (disease)",
          "leanness, inherited, autosomal recessive",
          "monogenic obesity",
          "obesity, association with, Autosomal recessive",
          "obesity, early-onset, susceptibility to, Autosomal recessive",
          "obesity, late-onset, Autosomal recessive",
          "obesity, mild, early-onset, Autosomal recessive",
          "obesity, severe, Autosomal recessive",
          "obesity, severe, and type II diabetes, Autosomal recessive",
          "obesity, susceptibility to, Autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 21,
      "reference_id": "MONDO:0019182"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19055,
      "label": "inherited obesity"
    }
  ]
}