{
  "id": 2701,
  "label": "alopecia, isolated",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000005",
  "properties": {
    "xrefs": [
      "OMIMPS:203655"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 8,
  "parents": [
    {
      "id": 6660,
      "label": "alopecia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19134
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:987",
          "ICD9:704.0",
          "ICD9:704.00",
          "ICD9:704.09",
          "MEDGEN:7982",
          "MESH:D000505",
          "NCIT:C50575",
          "Orphanet:79364",
          "SCTID:56317004",
          "UMLS:C0002170",
          "icd11.foundation:1313926062"
        ],
        "synonyms": [
          "alopecia",
          "hair loss",
          "loss Of hair",
          "alopecia areata"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Hair loss usually from the scalp. It may result in bald spots or spread to the entire scalp or the entire epidermis. It may be androgenetic or caused by chemotherapeutic agents, compulsive hair pulling, autoimmune disorders or congenital conditions."
      },
      "child_count": 26,
      "reference_id": "MONDO:0004907"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MESH:D012873",
          "SCTID:239001006"
        ],
        "synonyms": [
          "disease, genetic skin",
          "diseases, genetic skin",
          "genetic skin disease",
          "genetic skin diseases",
          "genodermatosis",
          "skin disease, genetic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of skin disease that is caused by a modification of the individual's genome."
      },
      "child_count": 228,
      "reference_id": "MONDO:0100118"
    }
  ],
  "children": [
    {
      "id": 8495,
      "label": "alopecia areata 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2701,
        7026
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015035",
          "MEDGEN:400208",
          "MESH:C566303",
          "OMIM:104000",
          "UMLS:C1863094"
        ],
        "synonyms": [
          "alopecia areata 1",
          "AA1",
          "alopecia universalis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0007082"
    },
    {
      "id": 8497,
      "label": "familial focal alopecia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2701
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024522",
          "MEDGEN:350835",
          "MESH:C566301",
          "OMIM:104110",
          "UMLS:C1863092"
        ],
        "synonyms": [
          "alopecia, familial focal",
          "ALPF"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0007084"
    },
    {
      "id": 8591,
      "label": "alopecia, androgenetic, 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2701,
        7025
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024530",
          "MEDGEN:886756",
          "OMIM:109200",
          "UMLS:C4049090"
        ],
        "synonyms": [
          "AGA1",
          "alopecia, androgenetic, 1",
          "baldness, Male pattern"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0007184"
    },
    {
      "id": 10030,
      "label": "alopecia universalis congenita",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2701
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050634",
          "GARD:0000614",
          "ICD9:704.09",
          "MEDGEN:349262",
          "MESH:C537055",
          "MedDRA:10001767",
          "OMIM:203655",
          "Orphanet:701",
          "SCTID:86166000",
          "UMLS:C1859877"
        ],
        "synonyms": [
          "alopecia universalis congenita",
          "atrichia, generalised",
          "atrichia, generalized",
          "ALUNC",
          "AU",
          "alopecia areata universalis",
          "alopecia universalis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "The most severe form of alopecia areata, an inflammatory disease of the hair follicle, which is characterized by a complete loss of hair of the scalp and all the hair-bearing areas of the body."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008757"
    },
    {
      "id": 11407,
      "label": "alopecia, congenital",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2701,
        18972
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0001470",
          "ICD10CM:Q84.0",
          "MEDGEN:78581",
          "MESH:C535981",
          "NCIT:C35790",
          "OMIM:300042",
          "SCTID:2965006",
          "UMLS:C0265992"
        ],
        "synonyms": [
          "alopecia, congenital",
          "congenital alopecia",
          "ALPC"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A congenital condition characterized by the absence of hair on the scalp or entire body. The lack of hair is rarely absolute and is usually accompanied by incompletely grown, lanugo-like hair. It affects males twice as much as females and a familial tendency is common."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010229"
    },
    {
      "id": 11571,
      "label": "alopecia, androgenetic, 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2701,
        7025
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024724",
          "MEDGEN:395522",
          "MESH:C567473",
          "OMIM:300710",
          "UMLS:C2678038"
        ],
        "synonyms": [
          "AGA2",
          "alopecia, androgenetic, 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010410"
    },
    {
      "id": 13599,
      "label": "alopecia areata 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2701,
        18972
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015496",
          "MEDGEN:343971",
          "MESH:C565186",
          "OMIM:610753",
          "UMLS:C1853104"
        ],
        "synonyms": [
          "AA2",
          "alopecia areata 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012551"
    },
    {
      "id": 13939,
      "label": "alopecia, androgenetic, 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2701,
        7025
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024897",
          "MEDGEN:382808",
          "MESH:C567317",
          "OMIM:612421",
          "UMLS:C2676272"
        ],
        "synonyms": [
          "AGA3",
          "alopecia, androgenetic, 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012899"
    }
  ],
  "roots": [
    {
      "id": 6660,
      "label": "alopecia"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}