{
  "id": 9335,
  "label": "monilethrix",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008009",
  "properties": {
    "xrefs": [
      "DOID:0050472",
      "GARD:0000093",
      "MEDGEN:108185",
      "MESH:D056734",
      "NCIT:C84894",
      "NORD:1454",
      "OMIMPS:158000",
      "Orphanet:573",
      "SCTID:69488000",
      "UMLS:C0546966",
      "icd11.foundation:415074833"
    ],
    "synonyms": [
      "monilethrix",
      "moniliform hair syndrome",
      "MNLIX",
      "nodose hair"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Monilethrix is a rare genodermatosis characterized by a hair shaft dysplasia resulting in hypotrichosis."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 2903,
      "label": "autosomal dominant disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050736",
          "ICD9:758.5",
          "MEDGEN:539206",
          "SCTID:11164009",
          "UMLS:C0265385"
        ],
        "synonyms": [
          "autosomal dominant disease or disorder",
          "autosomal dominant hereditary disorder",
          "autosomal dominant inherited disorder",
          "disease or disorder, autosomal dominant",
          "disease, autosomal dominant"
        ],
        "definition": "Autosomal dominant form of disease."
      },
      "child_count": 192,
      "reference_id": "MONDO:0000426"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MESH:D012873",
          "SCTID:239001006"
        ],
        "synonyms": [
          "disease, genetic skin",
          "diseases, genetic skin",
          "genetic skin disease",
          "genetic skin diseases",
          "genodermatosis",
          "skin disease, genetic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of skin disease that is caused by a modification of the individual's genome."
      },
      "child_count": 228,
      "reference_id": "MONDO:0100118"
    }
  ],
  "children": [
    {
      "id": 24715,
      "label": "monilethrix-2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9335
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061152",
          "GARD:0028015",
          "MEDGEN:1876490",
          "OMIM:621169",
          "UMLS:C6012713"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0700341"
    },
    {
      "id": 24716,
      "label": "monilethrix-3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9335
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061153",
          "GARD:0028016",
          "MEDGEN:1876497",
          "OMIM:621170",
          "UMLS:C6012714"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0700342"
    },
    {
      "id": 24717,
      "label": "monilethrix-1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9335
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061145",
          "GARD:0028017",
          "MEDGEN:1876529",
          "OMIM:158000",
          "UMLS:C6012688"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0700343"
    }
  ],
  "roots": [
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}