{
  "id": 10138,
  "label": "microcephalic osteodysplastic primordial dwarfism, type 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008873",
  "properties": {
    "xrefs": [
      "GARD:0015145",
      "MEDGEN:349167",
      "MESH:C537320",
      "OMIM:210730",
      "UMLS:C1859439"
    ],
    "synonyms": [
      "Mopd 3",
      "Mopd, Caroline Crachami type",
      "Mopd, Sicilian fairy type",
      "microcephalic osteodysplastic primordial dwarfism, Caroline Crachami type",
      "microcephalic osteodysplastic primordial dwarfism, Sicilian fairy type",
      "microcephalic osteodysplastic primordial dwarfism, type III",
      "osteodysplastic primordial dwarfism, type 3"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2712,
      "label": "microcephalic osteodysplastic primordial dwarfism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3394
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022705"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0000060"
    },
    {
      "id": 17405,
      "label": "microcephalic osteodysplastic primordial dwarfism types I and III",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        24802
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0005120",
          "MEDGEN:1380769",
          "Orphanet:2636",
          "SCTID:725461009",
          "UMLS:C4319565"
        ],
        "synonyms": [
          "MOPD types I and III",
          "microcephalic osteodysplastic primordial dwarfism, Taybi-Linder type",
          "primordial microcephalic dwarfism, Crachami type",
          "Taybi-Linder syndrome",
          "MOPD 1",
          "brachymelic primordial dwarfism",
          "cephaloskeletal dysplasia",
          "low-birth-weight dwarfism with skeletal dysplasia",
          "microcephalic osteodysplastic primordial dwarfism type 1",
          "microcephalic osteodysplastic primordial dwarfism types 1 and 3",
          "osteodysplastic primordial dwarfism type I"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Microcephalic osteodysplastic primordial dwarfism (MOPD) types 1 and 3 are characterized by intrauterine and postnatal growth retardation, microcephaly, facial dysmorphism, skeletal dysplasia, low-birth weight and brain anomalies. Although MOPD types 1 and 3 were originally described as two separate entities on the basis of radiological criteria (notably small differences in pelvic and long bone structure), later reports confirmed that the two forms represent different modes of expression of the same syndrome."
      },
      "child_count": 4,
      "reference_id": "MONDO:0016994"
    },
    {
      "id": 24226,
      "label": "Mendelian neurodevelopmental disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24270,
        24488
      ],
      "type_id": 0,
      "properties": {
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neurodevelopmental disorder that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 550,
      "reference_id": "MONDO:0100500"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2712,
      "label": "microcephalic osteodysplastic primordial dwarfism"
    },
    {
      "id": 17405,
      "label": "microcephalic osteodysplastic primordial dwarfism types I and III"
    },
    {
      "id": 24226,
      "label": "Mendelian neurodevelopmental disorder"
    }
  ]
}