{
  "id": 11810,
  "label": "syndromic X-linked intellectual disability Snyder type",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010664",
  "properties": {
    "xrefs": [
      "DOID:0060802",
      "GARD:0005615",
      "ICD9:758.89",
      "MEDGEN:162918",
      "MESH:C536678",
      "NORD:1890",
      "OMIM:309583",
      "Orphanet:3063",
      "SCTID:702416008",
      "UMLS:C0796160"
    ],
    "synonyms": [
      "SRS",
      "Snyder-Robinson Syndrome",
      "Snyder-Robinson intellectual disability syndrome",
      "Snyder-Robinson mental retardation syndrome",
      "Snyder-Robinson syndrome",
      "intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type, X-linked recessive",
      "intellectual disability, X-linked, Snyder-Robinson type",
      "syndromic X-linked intellectual disability Snyder type",
      "MRXSSR",
      "X-linked intellectual disability Snyder-Robinson type",
      "X-linked intellectual disability, Snyder type",
      "X-linked mental retardation Snyder-Robinson type",
      "intellectual disability, X-linked, syndromic, Snyder-Robinson type",
      "mental retardation, X-linked, syndromic, Snyder-Robinson type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Snyder-Robinson syndrome (SRS) is an X-linked intellectual disability syndrome, including also hypotonia, an unsteady gait, osteoporosis, kyphoscoliosis and facial asymmetry. Severe generalized psychomotor evolving to moderate to profound global intellectual disability is also observed."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19742,
      "label": "X-linked syndromic intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2961,
        24021
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060309",
          "OMIMPS:309510",
          "Orphanet:98464"
        ],
        "synonyms": [
          "X-linked syndromic intellectual disability",
          "intellectual disability, X-linked syndromic",
          "mental retardation, X-linked syndromic",
          "syndromic X-linked intellectual disability",
          "syndromic intellectual disability, X-linked"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A syndromic intellectual disability with an X-linked mode of inheritance."
      },
      "child_count": 162,
      "reference_id": "MONDO:0020119"
    },
    {
      "id": 24863,
      "label": "disorder of polyamine metabolism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24199
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026469"
        ],
        "definition": "An inherited metabolic disease that has its basis in the disruption of the polyamine metabolic process."
      },
      "child_count": 4,
      "reference_id": "MONDO:0800159"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19742,
      "label": "X-linked syndromic intellectual disability"
    },
    {
      "id": 24863,
      "label": "disorder of polyamine metabolism"
    }
  ]
}