{
  "id": 17419,
  "label": "interstitial lung disease specific to infancy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017019",
  "properties": {
    "xrefs": [
      "MEDGEN:1842984",
      "Orphanet:264694",
      "UMLS:C5679737"
    ],
    "synonyms": [
      "ILD specific to infancy"
    ],
    "categories": [
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "parents": [
    {
      "id": 17417,
      "label": "primary interstitial lung disease specific to childhood",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17416
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010559",
          "MEDGEN:853969",
          "Orphanet:264665",
          "UMLS:C3161253",
          "icd11.foundation:1408868257"
        ],
        "synonyms": [
          "primary ILD specific to childhood",
          "primary interstitial lung disease specific to childhood",
          "cHILD",
          "children's interstitial lung disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0017015"
    }
  ],
  "children": [
    {
      "id": 16872,
      "label": "pulmonary interstitial glycogenosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17419
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020516",
          "ICD10CM:J84.842",
          "MEDGEN:838075",
          "Orphanet:217557",
          "SCTID:707551007",
          "UMLS:C3161106",
          "icd11.foundation:1386580655"
        ],
        "synonyms": [
          "PIG",
          "infantile cellular interstitial pneumonitis",
          "pig"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "Pulmonary interstitial glycogenosis (PIG) is a rare non-lethal pediatric form of interstitial lung disease (ILD)."
      },
      "child_count": 0,
      "reference_id": "MONDO:0016321"
    },
    {
      "id": 16873,
      "label": "neuroendocrine cell hyperplasia of infancy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6775,
        17419
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020517",
          "ICD10CM:J84.841",
          "MEDGEN:837309",
          "NCIT:C120169",
          "Orphanet:217560",
          "SCTID:707435002",
          "UMLS:C3161105",
          "icd11.foundation:1641999159"
        ],
        "synonyms": [
          "CTI",
          "NCHI",
          "NEHI",
          "chronic tachypnoe of infancy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "Neuroendocrine cell hyperplasia of infancy (NCHI) is a non-lethal pediatric form of interstitial lung disease (ILD) characterized by tachypnea without respiratory failure."
      },
      "child_count": 0,
      "reference_id": "MONDO:0016322"
    },
    {
      "id": 19411,
      "label": "chronic pneumonitis of infancy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17419,
        20399
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019166",
          "MEDGEN:846677",
          "Orphanet:91359",
          "SCTID:708026002",
          "UMLS:C3872848",
          "icd11.foundation:1821220054"
        ],
        "synonyms": [
          "CPI"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "Chronic pneumonitis of infancy is a rare pediatric form of interstitial lung disease (ILD)."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019621"
    },
    {
      "id": 24819,
      "label": "persistent tachypnoe of infancy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17419
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026437"
        ],
        "synonyms": [
          "PTI"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "A interstial lung disease characterized by the presence of persistent or intermittent tachypnea (usually noticed in neonatal period or after an acute infection for the first time in first months of life), crackles in 86 %, retractions in 82%, failure to thrive in 66%, chest wall abnormalities in 22% and hypoxemia or desaturation in 88%."
      },
      "child_count": 2,
      "reference_id": "MONDO:0800109"
    },
    {
      "id": 24828,
      "label": "cellular interstitial pneumonitis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17419
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026441"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "An interstitial lung disease specific to infancy that is characterized by tachypnea at birth and persistent disease, diffuse interstitial thickening due to pale oval and spindle-shaped histiocytes without scarring."
      },
      "child_count": 0,
      "reference_id": "MONDO:0800121"
    }
  ],
  "roots": [
    {
      "id": 17417,
      "label": "primary interstitial lung disease specific to childhood"
    }
  ]
}