{
  "id": 14672,
  "label": "familial progressive hyperpigmentation",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013648",
  "properties": {
    "xrefs": [
      "GARD:0016706",
      "OMIM:614233",
      "Orphanet:79146",
      "SCTID:715630006",
      "icd11.foundation:1808730427"
    ],
    "synonyms": [
      "melanosis diffusa congenita",
      "melanosis universalis hereditaria",
      "universal melanosis",
      "FPH1",
      "Fph",
      "hyperpigmentation, familial progressive, 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Familial progressive hyperpigmentation is a rare, genetic, skin pigmentation anomaly disorder characterized by irregular patches of hyperpigmented skin which present at birth or in early infancy and increase in size, number and confluence with age. Affected areas of the body include the face, neck, trunk and limbs, as well as the palms, soles, oral mucosa and conjuctiva. No hypogmentation macules are observed and no systemic diseases are associated."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 19140,
      "label": "hyperpigmentation of the skin",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19139
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "HP:0000953",
          "ICD9:709.09",
          "MEDGEN:57992",
          "Orphanet:79375",
          "SCTID:49765009",
          "UMLS:C0162834"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 24,
      "reference_id": "MONDO:0019289"
    }
  ],
  "children": [
    {
      "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"
    }
  ],
  "roots": [
    {
      "id": 19140,
      "label": "hyperpigmentation of the skin"
    }
  ]
}