{
  "id": 14056,
  "label": "hypotrichosis 5",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013017",
  "properties": {
    "xrefs": [
      "DOID:0110702",
      "GARD:0015585",
      "MEDGEN:440568",
      "MESH:C567554",
      "OMIM:612841",
      "UMLS:C2748535"
    ],
    "synonyms": [
      "HYPT5",
      "MUHH2",
      "Marie Unna hereditary hypotrichosis 2",
      "Muhh2",
      "hypotrichosis 5",
      "hypotrichosis type 5",
      "hypt5"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "A hypotrichosis that has material basis in a mutation on chromosome 1p21.1-q21.3."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18628,
      "label": "Marie Unna hereditary hypotrichosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5030
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0003390",
          "MEDGEN:419706",
          "MESH:C535912",
          "Orphanet:444",
          "UMLS:C2931059"
        ],
        "synonyms": [
          "HR hypotrichosis",
          "MUHH",
          "Marie Unna congenital hypotrichosis",
          "hypotrichosis caused by mutation in HR",
          "hypotrichosis, Marie Unna type"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A rare autosomal dominant hair loss disorder characterized by the absence or scarcity of scalp hair, eyebrows, and eyelashes at birth; coarse and wiry hair during childhood; and progressive hair loss beginning around puberty."
      },
      "child_count": 2,
      "reference_id": "MONDO:0018631"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18628,
      "label": "Marie Unna hereditary hypotrichosis"
    }
  ]
}