{
  "id": 17577,
  "label": "familial progressive hyper- and hypopigmentation",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017239",
  "properties": {
    "xrefs": [
      "GARD:0017298",
      "MEDGEN:1643385",
      "Orphanet:280628",
      "UMLS:C4706423",
      "icd11.foundation:1229773662"
    ],
    "synonyms": [
      "FPHH"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Familial progressive hyper- and hypopigmentation is a rare, genetic, skin pigmentation anomaly disorder characterized by progressive, diffuse, partly blotchy, hyperpigmented lesions that are intermixed with multiple café-au-lait spots, hypopigmented maculae and lentigines and are located on the face, neck, trunk and limbs, as well as, frequently, the palms, soles and oral mucosa. Dispigmentation pattern can range from well isolated café-au-lait/hypopigmented patches on a background of normal-appearing skin to confetti-like or mottled appearance."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9120,
      "label": "hyperpigmentation with or without hypopigmentation, familial progressive",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        14672,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111373",
          "GARD:0018073",
          "MEDGEN:333550",
          "OMIM:145250",
          "UMLS:C1840392"
        ],
        "synonyms": [
          "hyperpigmentation with or without hypopigmentation",
          "hyperpigmentation with or without hypopigmentation, familial progressive",
          "macules, hereditary congenital hypopigmented and hyperpigmented",
          "melanosis, universal",
          "FPHH",
          "hyperpigmentation, familial progressive, 2",
          "hyperpigmentation, familial progressive, 2, formerly",
          "melanosis universalis hereditaria"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0007771"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9120,
      "label": "hyperpigmentation with or without hypopigmentation, familial progressive"
    }
  ]
}