{
  "id": 18285,
  "label": "minimal pigment oculocutaneous albinism type 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018136",
  "properties": {
    "xrefs": [
      "GARD:0021529",
      "ICD9:270.2",
      "MEDGEN:1842241",
      "Orphanet:352734",
      "SCTID:237919007",
      "UMLS:C5679923"
    ],
    "synonyms": [
      "MP OCA type 1",
      "OCA1-MP"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Type 1 minimal pigment oculocutaneous albinism (OCA1-MP) is an extremely rare form of OCA1 with minimal pigment present, characterized by blond hair, variable iris transillumination, visual acuity ranging from 20/80-20/200 and white skin, with or without skin nevi."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18284,
      "label": "oculocutaneous albinism type 1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17628,
        18837
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0004037",
          "MEDGEN:82809",
          "MESH:C537728",
          "Orphanet:352731",
          "SCTID:765146000",
          "UMLS:C0268494"
        ],
        "synonyms": [
          "OCA1",
          "oculocutaneous albinism type 1",
          "ATN",
          "oculocutaneous albinism, tyrosinase negative"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Type 1 oculocutaneous albinism (OCA1) describes a group of tyrosine related OCAs that includes OCA1A, OCA1B, type 1 minimal pigment oculocutaneous albinism (OCA1-MP) and type 1 temperature sensitive oculocutaneous albinism (OCA1-TS)."
      },
      "child_count": 6,
      "reference_id": "MONDO:0018135"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18284,
      "label": "oculocutaneous albinism type 1"
    }
  ]
}