{
  "id": 16093,
  "label": "amniotic band syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015167",
  "properties": {
    "xrefs": [
      "GARD:0000429",
      "MEDGEN:66322",
      "MESH:D000652",
      "NCIT:C84552",
      "NORD:766",
      "OMIM:217100",
      "Orphanet:1034",
      "Orphanet:295000",
      "SCTID:440214006",
      "UMLS:C0220724",
      "icd11.foundation:1033549095"
    ],
    "synonyms": [
      "Adam syndrome",
      "Streeter dysplasia",
      "amniotic band constriction",
      "amniotic bands",
      "amniotic deformity-adhesion-mutilation syndrome",
      "congenital ring constrictions",
      "constriction band syndrome",
      "constriction rings syndrome",
      "deformity due to amniotic band",
      "Adam Complex",
      "CONSTRICTING bands, congenital",
      "Streeter anomaly",
      "amniotic band sequence",
      "amniotic bands sequence",
      "amputation, congenital",
      "congenital constricting bands",
      "familial amniotic bands",
      "terminal transverse defects of arm"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "A group of sporadic congenital anomalies, that occur in association with amniotic bands, involving the limbs, craniofacial regions, spine and trunk with a highly variable clinical spectrum ranging from simple digital band constriction (or amputation) to complex craniofacial, central nervous system and visceral anomalies."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 18360,
      "label": "skeletal dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        7061
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:98053",
          "Orphanet:364526",
          "UMLS:C0410528"
        ],
        "synonyms": [
          "Mendelian skeletal dysplasia",
          "primary bone dysplasia",
          "primary osteodysplasia",
          "primary skeletal dysplasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Any Mendelian diseases that affects growth and development of the skeleton."
      },
      "child_count": 238,
      "reference_id": "MONDO:0018230"
    },
    {
      "id": 18362,
      "label": "dysostosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7153
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1934",
          "ICD9:756.9",
          "MEDGEN:4430",
          "MESH:D004413",
          "NCIT:C34560",
          "Orphanet:364559",
          "SCTID:109420003",
          "UMLS:C0013393"
        ],
        "synonyms": [
          "dysostosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A group of disorders in which the skeletal involvement is predominantly manifested as abnormalities of individual bones or in a group of bones."
      },
      "child_count": 108,
      "reference_id": "MONDO:0018234"
    }
  ],
  "children": [
    {
      "id": 19511,
      "label": "terminal transverse defects of arm",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16093
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025145",
          "MEDGEN:341800",
          "MESH:C565681",
          "Orphanet:93937",
          "UMLS:C1857578"
        ],
        "synonyms": [
          "congenital limb amputation"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0019760"
    }
  ],
  "roots": [
    {
      "id": 18360,
      "label": "skeletal dysplasia"
    },
    {
      "id": 18362,
      "label": "dysostosis"
    }
  ]
}