{
  "id": 15256,
  "label": "familial hyperprolactinemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014250",
  "properties": {
    "xrefs": [
      "GARD:0017634",
      "MEDGEN:1645317",
      "OMIM:615555",
      "Orphanet:397685",
      "SCTID:763715007",
      "UMLS:C4706551"
    ],
    "synonyms": [
      "familial hyperprolactinemia",
      "familial isolated prolactin receptor deficiency",
      "hereditary hyperprolactinemia (disease)",
      "HPRL",
      "hyperprolactinemia"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Familial hyperprolactinemia is a rare, genetic endocrine disorder characterized by persistently high prolactin serum levels (not associated with gestation, puerperium, drug intake or pituitary tumor) in multiple affected family members. Clinically it manifests with signs usually observed in hyperprolactinemia, which are: secondary medroxyprogesterone acetate (MPA)-negative amenorrhea and galactorrhea in female patients, and hypogonadism and decreased testosterone level-driven sexual disfunction in male patients. Oligomenorrhea and primary infertility have also been reported in some female patients."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7420,
      "label": "hyperprolactinemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8241
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0007319",
          "HP:0000870",
          "ICD10CM:E22.1",
          "ICD9:253.1",
          "MEDGEN:5698",
          "MESH:D006966",
          "NANDO:2100115",
          "NANDO:2200322",
          "SCTID:237662005",
          "UMLS:C0020514"
        ],
        "synonyms": [
          "hyperprolactinaemia",
          "hyperprolactinemia",
          "hyperprolactinemia (disease)",
          "hyperprolactinemias",
          "hypersecretion syndrome, prolactin",
          "inappropriate prolactin secretion",
          "inappropriate prolactin secretion syndrome",
          "inappropriate secretion prolactin",
          "prolactin hypersecretion syndrome",
          "prolactin secretion, inappropriate",
          "prolactin, inappropriate secretion",
          "secretion prolactin, inappropriate",
          "secretion, inappropriate prolactin",
          "syndrome, prolactin hypersecretion"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Abnormally high level of prolactin in the blood."
      },
      "child_count": 2,
      "reference_id": "MONDO:0005804"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7420,
      "label": "hyperprolactinemia"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}