{
  "id": 6660,
  "label": "alopecia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004907",
  "properties": {
    "xrefs": [
      "DOID:987",
      "ICD9:704.0",
      "ICD9:704.00",
      "ICD9:704.09",
      "MEDGEN:7982",
      "MESH:D000505",
      "NCIT:C50575",
      "Orphanet:79364",
      "SCTID:56317004",
      "UMLS:C0002170",
      "icd11.foundation:1313926062"
    ],
    "synonyms": [
      "alopecia",
      "hair loss",
      "loss Of hair",
      "alopecia areata"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Hair loss usually from the scalp. It may result in bald spots or spread to the entire scalp or the entire epidermis. It may be androgenetic or caused by chemotherapeutic agents, compulsive hair pulling, autoimmune disorders or congenital conditions."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 26,
  "parents": [
    {
      "id": 19134,
      "label": "hair anomaly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4924,
        21436
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:539624",
          "Orphanet:79363",
          "UMLS:C0265991"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 16,
      "reference_id": "MONDO:0019278"
    }
  ],
  "children": [
    {
      "id": 2701,
      "label": "alopecia, isolated",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6660,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "OMIMPS:203655"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 16,
      "reference_id": "MONDO:0000005"
    },
    {
      "id": 4282,
      "label": "telogen effluvium",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1943",
          "GARD:0023077",
          "ICD10CM:L65.0",
          "ICD9:704.02",
          "MEDGEN:537938",
          "NCIT:C112200",
          "SCTID:39479004",
          "UMLS:C0263518",
          "icd11.foundation:1188535025"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A scalp hair loss condition characterized by excessive shedding of hair in the resting phase of growth, usually following a fever or major body stress."
      },
      "child_count": 0,
      "reference_id": "MONDO:0002153"
    },
    {
      "id": 7026,
      "label": "alopecia areata",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:986",
          "EFO:0004192",
          "ICD10CM:L63",
          "ICD10WHO:L63",
          "ICD9:704.01",
          "MEDGEN:213",
          "MESH:D000506",
          "SCTID:68225006",
          "UMLS:C0002171",
          "icd11.foundation:65720611"
        ],
        "synonyms": [
          "alopecia areata",
          "alopecia circumscripta",
          "patchy loss of hair"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Loss of scalp and body hair involving microscopically inflammatory patchy areas."
      },
      "child_count": 2,
      "reference_id": "MONDO:0005340"
    },
    {
      "id": 7139,
      "label": "chemotherapy-induced alopecia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0005400",
          "GARD:0024192",
          "MEDGEN:1720394",
          "NCIT:C164162",
          "UMLS:C5236021"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Hair loss as a result of chemotherapy treatment."
      },
      "child_count": 0,
      "reference_id": "MONDO:0005483"
    },
    {
      "id": 8034,
      "label": "alopecia mucinosa",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6660,
        8082,
        20705
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9905",
          "EFO:1000701",
          "GARD:0024437",
          "ICD10CM:L65.2",
          "ICD9:704.09",
          "MEDGEN:1419",
          "MESH:D000507",
          "NCIT:C82859",
          "PMID:24350019",
          "SCTID:27382006",
          "UMLS:C0002173"
        ],
        "synonyms": [
          "alopecia Mucinosa",
          "alopecia mucinosa",
          "alopecia mucinosis",
          "cutaneous focal mucinosis of hair follicle",
          "hair follicle cutaneous focal mucinosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A rare dermatologic disorder characterized by the accumulation of mucinous material in the hair follicles. In some cases it is associated with lymphoproliferative disorders, most often mycosis fungoides and Hodgkin lymphoma."
      },
      "child_count": 0,
      "reference_id": "MONDO:0006551"
    },
    {
      "id": 10114,
      "label": "atrichia with papular lesions",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5714,
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060689",
          "GARD:0016762",
          "MEDGEN:395299",
          "MESH:C565924",
          "OMIM:209500",
          "Orphanet:86819",
          "SCTID:715963002",
          "UMLS:C1859592"
        ],
        "synonyms": [
          "atrichia with papular lesions",
          "papular atrichia",
          "APL"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Atrichia with papular lesions is a rare inherited form of alopecia characterized by irreversible hair loss during the neonatal period on all hear-bearing areas of the body, later associated with the development of papular lesions all over the body and preferentially on the face and extensor surfaces of the extremities."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008847"
    },
    {
      "id": 12041,
      "label": "loose anagen syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6660,
        20383
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111702",
          "GARD:0003287",
          "ICD9:704.8",
          "MEDGEN:98351",
          "MESH:D058247",
          "OMIM:600628",
          "Orphanet:168",
          "SCTID:238735005",
          "UMLS:C0406468",
          "icd11.foundation:547259783"
        ],
        "synonyms": [
          "loose anagen hair syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Loose anagen syndrome is a rare benign hair disorder affecting predominantly blond females in childhood and characterized by the presence of hair that can be easily and painlessly pulled out. Most of the hair is in the anagen phase and lacks an external epithelial sheath. Hair grows back quickly and the condition improves spontaneously with aging. Loose anagen hair can be associated with other anomalies, such as coloboma."
      },
      "child_count": 2,
      "reference_id": "MONDO:0010908"
    },
    {
      "id": 12055,
      "label": "Satoyoshi syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6660,
        6756,
        19578
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000160",
          "MEDGEN:318882",
          "MESH:C536616",
          "MedDRA:10070579",
          "OMIM:600705",
          "Orphanet:3130",
          "SCTID:763630007",
          "UMLS:C1833454"
        ],
        "synonyms": [
          "Komuragaeri disease",
          "Satoyoshi syndrome",
          "muscle spasms, intermittent with alopecia, diarrhea and skeletal abnormalities",
          "muscle spasms, intermittent with alopecia, diarrhoea and skeletal abnormalities",
          "muscle spasms, intermittent, with alopecia, diarrhea, and skeletal abnormalities"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Satoyoshi syndrome is a rare syndrome characterized by progressive, painful, intermittent muscle spasms. These muscle spasms usually start between 6-15 years old. Other symptoms of the syndrome may include diarrhea and an inability of the digestive tract to absorb certain foods, especially carbohydrates (malabsorption). People affected by Satoyoshi syndrome may also have loss of hair on the head and body (alopecia universalis), short stature, and skeletal abnormalities. Women with Satoyoshi syndrome may not have a menstrual cycle (amenorrhea). In all published cases, only one person in a family has Satoyoshi syndrome. This is even true when the person with Satoyoshi syndrome comes from a large family. Satoyoshi syndrome seems to be more common in Japan. The exact cause of the syndrome is unknown, but some researchers think it may be an autoimmune disease. Satoyoshi syndrome can be diagnosed when a doctor sees symptoms that are consistent with the syndrome. The diagnosis can be confirmed by a variety of laboratory tests. Treatment for Satoyoshi syndrome includes medication to suppress the immune system."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010922"
    },
    {
      "id": 12145,
      "label": "alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016553",
          "MEDGEN:321990",
          "MESH:C563370",
          "OMIM:601217",
          "Orphanet:1014",
          "SCTID:720981000",
          "UMLS:C1832593"
        ],
        "synonyms": [
          "Devriendt-Vandenberghe-Fryns syndrome",
          "alopecia-intellectual disability syndrome with convulsions and hypergonadotropic hypogonadism",
          "alopecia-mental retardation syndrome with convulsions and hypergonadotropic hypogonadism"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "This syndrome is characterized by the association of total alopecia (present at birth), mild intellectual deficit and hypergonadotropic hypogonadism."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011019"
    },
    {
      "id": 14173,
      "label": "hereditary hypotrichosis with recurrent skin vesicles",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5714,
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017124",
          "MEDGEN:442697",
          "MESH:C567751",
          "OMIM:613102",
          "Orphanet:217407",
          "SCTID:724350009",
          "UMLS:C2751292"
        ],
        "synonyms": [
          "hereditary hypotrichosis with recurrent skin vesicles",
          "hypotrichosis and recurrent skin vesicles"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Hereditary hypotrichosis with recurrent skin vesicles is a very rare inherited hair loss disorder described in a family and characterized by sparse, fragile or absent hair on the scalp, eyebrows, eyelashes, axillae and rest of the body, associated with vesicle formation on various parts of the scalp and body which regularly burst and release watery fluid."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013136"
    },
    {
      "id": 16051,
      "label": "alopecia antibody deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018713",
          "MEDGEN:1683018",
          "Orphanet:1006",
          "UMLS:C5190867"
        ],
        "synonyms": [
          "IPP-Gelfand syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0015082"
    },
    {
      "id": 16145,
      "label": "pseudopelade of Brocq",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0004536",
          "ICD9:704.09",
          "MEDGEN:88640",
          "Orphanet:129",
          "SCTID:238731001",
          "UMLS:C0086873"
        ],
        "synonyms": [
          "Brocq pseudopelade",
          "pseudo pelade of Brocq",
          "pseudo-pelade of Brocq"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Pseudo-pelade of Brocq is a rare hair abnormality characterized by onset in adulthood of soft, irregular, flesh-toned patches of alopecia primarily in the parietal and vertex portions of the scalp, without follicular hyperkeratosis or perifollicular inflammation."
      },
      "child_count": 0,
      "reference_id": "MONDO:0015261"
    },
    {
      "id": 17218,
      "label": "frontal fibrosing alopecia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010886",
          "MEDGEN:899012",
          "Orphanet:254492",
          "SCTID:717055000",
          "UMLS:C4255374",
          "icd11.foundation:1257078333"
        ],
        "synonyms": [
          "FFA"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Frontal fibrosing alopecia (FFA) is a rare variant of lichen planopilaris characterized by symmetrical, progressive, band-like anterior hair loss of the scalp."
      },
      "child_count": 0,
      "reference_id": "MONDO:0016776"
    },
    {
      "id": 18262,
      "label": "Quinquaud's folliculitis decalvans",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000373",
          "ICD9:704.09",
          "MEDGEN:750617",
          "Orphanet:346",
          "SCTID:53593008",
          "UMLS:C2608043",
          "icd11.foundation:1454811046"
        ],
        "synonyms": [
          "Quinquaud's decalvans folliculitis",
          "Quinquaud's disease",
          "Quinquaud’s disease",
          "folliculitis decalvans"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Folliculitis decalvans is a rare chronic inflammatory cicatricial alopecia of the scalp occurring in middle-aged adults and characterized by the development of alopecic patches with slowly centrifugal spread predominantly in the vertex and occipital area of the scalp, associated with perifollicular erythema, follicular pustules and hemorrhagic crusts."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018103"
    },
    {
      "id": 18794,
      "label": "Graham Little-Piccardi-Lassueur syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0003195",
          "MEDGEN:905915",
          "Orphanet:505",
          "SCTID:718215008",
          "UMLS:C4273658"
        ],
        "synonyms": [
          "Graham Little syndrome",
          "Piccardi-Lassueur-Little syndrome",
          "Graham-Little-Piccardi-Lassueur syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Graham Little-Piccardi-Lassueur syndrome is a variant of lichen planopilaris characterized by the clinical triad of progressive cicatricial (scarring) alopecia of the scalp, follicular keratotic papules on glabrous skin, and variable alopecia of the axillae and groin."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018858"
    },
    {
      "id": 18811,
      "label": "lichen planopilaris",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0003247",
          "ICD10CM:L66.1",
          "MEDGEN:44150",
          "MESH:C535892",
          "Orphanet:525",
          "SCTID:64540004",
          "UMLS:C0023645",
          "icd11.foundation:572258139"
        ],
        "synonyms": [
          "LPP",
          "follicular lichen planus",
          "lichen follicularis",
          "lichen planus follicularis",
          "Kossard disease",
          "frontal fibrosing alopecia (subtype)",
          "lichen planopilaris classic type"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Lichen planopilaris (LPP) is a rare cutaneous variant of lichen planus which affects hair follicles. It may occur on its own or in association with more common forms of lichen planus, usually classical type and/or oral lichen planus."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018879"
    },
    {
      "id": 18841,
      "label": "hypotrichosis simplex",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009170",
          "MEDGEN:344257",
          "MESH:C537160",
          "Orphanet:55654",
          "SCTID:723362004",
          "UMLS:C1854310"
        ],
        "synonyms": [
          "hereditary hypotrichosis simplex"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Hypotrichosis simplex (HS) or hereditary hypotrichosis simplex (HHS) is characterized by reduced pilosity over the scalp and body (with sparse, thin, and short hair) in the absence of other anomalies."
      },
      "child_count": 8,
      "reference_id": "MONDO:0018914"
    },
    {
      "id": 18972,
      "label": "alopecia totalis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000613",
          "ICD9:704.09",
          "MEDGEN:75525",
          "MedDRA:10001766",
          "Orphanet:700",
          "SCTID:19754005",
          "UMLS:C0263504",
          "icd11.foundation:1633035058"
        ],
        "synonyms": [
          "alopecia totalis",
          "total alopecia areata"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Alopecia totalis is a form of alopecia areata, an inflammatory disease of the hair follicle, characterized by a complete loss of hair of the entire scalp which becomes glabrous."
      },
      "child_count": 2,
      "reference_id": "MONDO:0019080"
    },
    {
      "id": 19380,
      "label": "hypotrichosis simplex of the scalp",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016789",
          "Orphanet:90368",
          "SCTID:717256009"
        ],
        "synonyms": [
          "hereditary hypotrichosis simplex of the scalp"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp."
      },
      "child_count": 2,
      "reference_id": "MONDO:0019575"
    },
    {
      "id": 20426,
      "label": "endocrine alopecia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025300",
          "ICD9:704.09",
          "MEDGEN:507423",
          "SCTID:54539003",
          "UMLS:C0002176"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 1,
      "reference_id": "MONDO:0021208"
    },
    {
      "id": 20767,
      "label": "alopecia universalis onychodystrophy vitiligo",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6660,
        9939
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000615",
          "MEDGEN:444049",
          "MESH:C537056",
          "UMLS:C2931408"
        ],
        "synonyms": [
          "alopecia universalis, onychodystrophy, and total vitiligo"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A syndrome characterized by total alopecia (hair loss), total vitíligo, and nail changes. The nail changes consist of fine pitting, associated with softness, and friability and may include horizontal splitting. The vitiligo is characterized by complete, rapid uniform loss of pigment which occurs without going through a patchy state. The entire cutaneous surface is light and translucent-appearing and is prone to burning on exposure to the sun."
      },
      "child_count": 0,
      "reference_id": "MONDO:0021851"
    },
    {
      "id": 20820,
      "label": "central centrifugal cicatricial alopecia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5714,
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010826",
          "ICD9:704.09",
          "MEDGEN:698033",
          "OMIM:618352",
          "SCTID:109441000119102",
          "UMLS:C1274708"
        ],
        "synonyms": [
          "central centrifugal cicatricial alopecia",
          "CCCA",
          "CENTRAL CENTRIFUGAL CICATRICIAL ALOPECIA",
          "central centrifugal alopecia",
          "hot comb alopecia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0022113"
    },
    {
      "id": 21110,
      "label": "ectodermal dysplasia alopecia preaxial polydactyly",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6660,
        19138
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0002040",
          "MEDGEN:419138",
          "MESH:C538016",
          "UMLS:C2931691"
        ],
        "synonyms": [
          "absence of body & scalp hair, rounded nails, thin dental enamel, preaxial polydactyly of the feet, and unusual facial appearance"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0023043"
    },
    {
      "id": 23089,
      "label": "Slti-Salem syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4278,
        4370,
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025851",
          "MEDGEN:419036",
          "MESH:C536673",
          "UMLS:C2931284"
        ],
        "synonyms": [
          "Slti Salem syndrome",
          "hypogonadism and frontoparietal alopecia",
          "hypogonadotropic hypogonadism alopecia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0042962"
    },
    {
      "id": 23140,
      "label": "microcephaly sparse hair intellectual disability seizures",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3608,
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025856",
          "MEDGEN:444077",
          "MESH:C537545",
          "UMLS:C2931530"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0043139"
    },
    {
      "id": 24880,
      "label": "alopecia universalis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5714,
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026477",
          "ICD10CM:L63.1",
          "MEDGEN:120481",
          "UMLS:C0263505",
          "icd11.foundation:69070500"
        ],
        "synonyms": [
          "AU"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0800198"
    }
  ],
  "roots": [
    {
      "id": 19134,
      "label": "hair anomaly"
    }
  ]
}