{
  "id": 2703,
  "label": "colorblindness, partial",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000014",
  "properties": {
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 3891,
      "label": "color vision disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20325
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13399",
          "ICD10CM:H53.5",
          "ICD9:368.5",
          "ICD9:368.59",
          "MEDGEN:1826147",
          "NCIT:C3891",
          "Orphanet:98658",
          "SCTID:193683001",
          "UMLS:C5681659"
        ],
        "synonyms": [
          "blindness color",
          "blindness colour",
          "color blindness",
          "color vision defects",
          "color vision deficiency",
          "color-vision disease",
          "colour vision defects"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "The absence of or defect in the perception of colors."
      },
      "child_count": 5,
      "reference_id": "MONDO:0001703"
    }
  ],
  "children": [
    {
      "id": 11718,
      "label": "red-green color blindness",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2703,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13909",
          "EFO:0005581",
          "GARD:0027795",
          "ICD10CM:H53.53",
          "ICD9:368.52",
          "MEDGEN:102324",
          "OMIM:303800",
          "Orphanet:319698",
          "SCTID:77479002",
          "UMLS:C0155016"
        ],
        "synonyms": [
          "Deutan defect",
          "colorblindness, deutan",
          "deuteranopia",
          "partial achromatopsia, deutan type",
          "CBD",
          "Deutan colorblindness",
          "Deuteranomaly",
          "Green colorblindness",
          "colorblindness, partial, DEUTAN series"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Deuteranopia is a type of color vision deficiency where the green photoreceptors are absent. It affects hue discrimination in the same way as protanopia, but without the dimming effect. Like protanopia, it is hereditary, sex-linked, and found in about 1% of the male population."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010564"
    }
  ],
  "roots": [
    {
      "id": 3891,
      "label": "color vision disorder"
    }
  ]
}