{
  "id": 7030,
  "label": "hypospadias",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0005345",
  "properties": {
    "xrefs": [
      "DOID:10892",
      "EFO:0004209",
      "HP:0000047",
      "ICD10CM:Q54",
      "ICD9:752.61",
      "MEDGEN:163083",
      "MESH:D007021",
      "NCIT:C40341",
      "OMIMPS:300633",
      "Orphanet:440",
      "SCTID:416010008",
      "UMLS:C0848558",
      "icd11.foundation:810247271"
    ],
    "synonyms": [
      "hypospadias",
      "hypospadias (disease)",
      "hypospadias familial"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      }
    ],
    "definition": "Hypospadias is the displacement of the urethral meatus on the ventrum of the penis. This abnormality is associated with a varyingly bent, twisted penis and opened dorsal prepuce."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "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": 6772,
      "label": "reproductive system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:15",
          "EFO:0000512",
          "MEDGEN:61253",
          "NCIT:C4875",
          "SCTID:362968007",
          "UMLS:C0178829",
          "Wikipedia:Reproductive_system_disease"
        ],
        "synonyms": [
          "disease of reproductive system",
          "disease or disorder of reproductive system",
          "disorder of reproductive system",
          "genital disorders",
          "reproductive disease",
          "reproductive system disease",
          "reproductive system disease or disorder",
          "reproductive system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "A disease involving the reproductive system."
      },
      "child_count": 30,
      "reference_id": "MONDO:0005039"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29380
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD10CM:Q00-Q99",
          "MEDGEN:1843482",
          "UMLS:C0694457"
        ],
        "definition": "Any disease or disorder that disrupts the process development of an anatomical structure. Can be due to genetic or environmental causes. Typically happens during embryogenesis, but also includes post-embryonic development."
      },
      "child_count": 190,
      "reference_id": "MONDO:0021147"
    }
  ],
  "children": [
    {
      "id": 9145,
      "label": "hypospadias 3, autosomal",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7030
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018184",
          "MEDGEN:382538",
          "MESH:C567191",
          "OMIM:146450",
          "UMLS:C2675154"
        ],
        "synonyms": [
          "hypospadias 3, autosomal",
          "hypospadias 3, autosomal, multifactorial",
          "HYSP3"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0007802"
    },
    {
      "id": 11547,
      "label": "hypospadias 1, X-linked",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7030
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018185",
          "MEDGEN:394735",
          "MESH:C567482",
          "OMIM:300633",
          "UMLS:C2678098"
        ],
        "synonyms": [
          "hypospadias 1, X-linked",
          "hypospadias 1, X-linked, X-linked recessive",
          "HYSP1"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010384"
    },
    {
      "id": 11583,
      "label": "hypospadias 2, X-linked",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7030
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018186",
          "MEDGEN:437064",
          "MESH:C567462",
          "OMIM:300758",
          "UMLS:C2677879"
        ],
        "synonyms": [
          "hypospadias 2, X-linked",
          "hypospadias 2, X-linked, X-linked recessive",
          "HYSP2"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010423"
    },
    {
      "id": 11617,
      "label": "hypospadias 4, X-linked",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7030
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018187",
          "MEDGEN:477089",
          "OMIM:300856",
          "UMLS:C3275458"
        ],
        "synonyms": [
          "HYSP4",
          "hypospadias 4, X-linked, susceptibility to"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010458"
    },
    {
      "id": 22913,
      "label": "isolated female hypospadias",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7030
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022434",
          "MEDGEN:1842898",
          "Orphanet:603515",
          "UMLS:C5681495"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0035821"
    }
  ],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 6772,
      "label": "reproductive system disorder"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis"
    }
  ]
}