{
  "id": 11718,
  "label": "red-green color blindness",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010564",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2703,
      "label": "colorblindness, partial",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3891
      ],
      "type_id": 0,
      "properties": {
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 1,
      "reference_id": "MONDO:0000014"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2703,
      "label": "colorblindness, partial"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}