{
  "id": 23567,
  "label": "Noonan syndrome-like disorder with loose anagen hair 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0054588",
  "properties": {
    "xrefs": [
      "DOID:0080693",
      "GARD:0025953",
      "MEDGEN:1376945",
      "NCIT:C176940",
      "OMIM:617506",
      "UMLS:C4479577"
    ],
    "synonyms": [
      "Noonan syndrome-like disorder with loose anagen hair 2",
      "NSLH2"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 12975,
      "label": "Noonan syndrome-like disorder with loose anagen hair",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        12041,
        16088,
        19780
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080691",
          "GARD:0010719",
          "MEDGEN:334697",
          "MESH:C564342",
          "NCIT:C178129",
          "OMIMPS:607721",
          "Orphanet:2701",
          "SCTID:723444009",
          "UMLS:C1843181"
        ],
        "synonyms": [
          "NS/LAH",
          "Noonan syndrome-like disorder with loose anagen hair",
          "Tosti syndrome",
          "NSLH",
          "NSLH1",
          "Noonan syndrome-like disorder with loose anagen hair 1",
          "Noonan-like syndrome with loose anagen hair"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Noonan-like syndrome with loose anagen hair (NS/LAH) is a Noonan-related syndrome, characterized by facial anomalies suggestive of Noonan syndrome ; a distinctive hair anomaly described as loose anagen hair syndrome ; frequent congenital heart defects; distinctive skin features with darkly pigmented skin, keratosis pilaris, eczema or occasional neonatal ichtyosis ; and short stature, often associated with a GH deficiency and psychomotor delays."
      },
      "child_count": 6,
      "reference_id": "MONDO:0011899"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 12975,
      "label": "Noonan syndrome-like disorder with loose anagen hair"
    }
  ]
}