{
  "id": 2706,
  "label": "infantile liver failure",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000023",
  "properties": {
    "xrefs": [
      "DOID:0080716",
      "GARD:0017820",
      "MEDGEN:1813021",
      "OMIMPS:615438",
      "Orphanet:464724",
      "UMLS:C5681094"
    ],
    "synonyms": [
      "fever-associated acute infantile liver failure syndrome",
      "infantile liver failure syndrome",
      "liver failure, infantile"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 4,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 23933,
      "label": "liver failure",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6878
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:88444",
          "MESH:D017093",
          "NCIT:C26922",
          "UMLS:C0085605"
        ],
        "synonyms": [
          "hepatic failure"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A liver disease characterized by the liver losing or has lost all of its function."
      },
      "child_count": 3,
      "reference_id": "MONDO:0100192"
    }
  ],
  "children": [
    {
      "id": 14149,
      "label": "acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2706,
        16918,
        19350
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080778",
          "GARD:0010593",
          "MEDGEN:480294",
          "OMIM:613070",
          "Orphanet:217371",
          "UMLS:C3278664"
        ],
        "synonyms": [
          "acute infantile liver failure",
          "LFIT",
          "TRMU infantile liver failure",
          "acute infantile liver failure due to synthesis defect of mitochondrial DNA-encoded proteins",
          "acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins",
          "infantile liver failure caused by mutation in TRMU",
          "liver failure, infantile, transient",
          "liver failure, transient infantile",
          "transient infantile liver failure"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Acute infantile liver failure due to mtDNA-encoded proteins synthesis defect is a very rare mitochondrial respiratory chain deficiency described in fewer than 10 infants, primarily of middle Eastern descent, and characterized clinically by transient but life-threatening liver failure with elevated liver enzymes, jaundice, vomiting, coagulopathy, hyperbilirubinemia, and lactic acidemia."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013111"
    },
    {
      "id": 15654,
      "label": "infantile liver failure syndrome 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2706
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0013113",
          "MEDGEN:815981",
          "NCIT:C158135",
          "OMIM:616483",
          "UMLS:C3809651"
        ],
        "synonyms": [
          "ILFS2",
          "NBAS infantile liver failure",
          "infantile liver failure caused by mutation in NBAS",
          "infantile liver failure syndrome 2",
          "infantile liver failure syndrome type 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any infantile liver failure in which the cause of the disease is a mutation in the NBAS gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014659"
    },
    {
      "id": 21513,
      "label": "infantile liver failure syndrome 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2706
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080717",
          "GARD:0013114",
          "MEDGEN:815852",
          "OMIM:615438",
          "Orphanet:370088",
          "UMLS:C3809522"
        ],
        "synonyms": [
          "LARS infantile liver failure",
          "Lars infantile liver failure",
          "infantile liver failure caused by mutation in LARS",
          "infantile liver failure caused by mutation in Lars",
          "infantile liver failure syndrome 1",
          "infantile liver failure syndrome type 1",
          "ILFS1",
          "acute infantile liver failure - multisystemic involvement syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Any infantile liver failure in which the cause of the disease is a mutation in the LARS gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0024568"
    },
    {
      "id": 22499,
      "label": "infantile liver failure syndrome 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2706
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016483",
          "MEDGEN:1684678",
          "OMIM:618641",
          "UMLS:C5231437"
        ],
        "synonyms": [
          "ILFS3",
          "INFANTILE LIVER FAILURE SYNDROME 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032844"
    }
  ],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 23933,
      "label": "liver failure"
    }
  ]
}