{
  "id": 16888,
  "label": "palmoplantar keratoderma-spastic paralysis syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016353",
  "properties": {
    "xrefs": [
      "GARD:0003095",
      "MEDGEN:444152",
      "MESH:C538358",
      "Orphanet:2201",
      "UMLS:C2931828"
    ],
    "synonyms": [
      "Powell-Venencie-Gordon syndrome",
      "palmoplantar hyperkeratosis-spastic paralysis syndrome",
      "keratoderma palmoplantar spastic paralysis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "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": 9189,
      "label": "palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        17917
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017977",
          "MEDGEN:322722",
          "MESH:C536153",
          "OMIM:148360",
          "Orphanet:538574",
          "UMLS:C1835671"
        ],
        "synonyms": [
          "keratoderma, palmoplantar, with nail dystrophy and hereditary motor-sensory neuropathy",
          "Charcot-Marie-Tooth disease with palmoplantar keratoderma and nail dystrophy",
          "axonal neuropathy with palmoplantar keratoderma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0007853"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 9189,
      "label": "palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome"
    }
  ]
}