{ "id": 3036, "label": "bone benign neoplasm", "model": { "label": "Mondo Disease Ontology (MONDO)", "source": 0 }, "type_id": 0, "reference_id": "MONDO:0000631", "properties": { "xrefs": [ "DOID:0060094", "GARD:0022813", "ICD9:213.9", "MEDGEN:146337", "NCIT:C4880", "SCTID:92027006", "UMLS:C0684516" ], "synonyms": [ "benign bone neoplasm", "benign bone tumor", "benign bone tumour", "benign neoplasm of bone", "benign neoplasm of the bone", "benign osseous neoplasm", "benign osseous tumor", "benign osseous tumour", "benign tumor of bone", "benign tumor of the bone", "benign tumour of bone", "benign tumour of the bone", "bone tissue benign neoplasm" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" } ], "definition": "A neoplasm that arises from the bone or articular cartilage and does not invade adjacent tissues or metastasize to other anatomic sites." }, "isLeaf": false, "isRoot": false, "child_count": 19, "parents": [ { "id": 3054, "label": "benign connective and soft tissue neoplasm", "isLeaf": false, "isRoot": false, "parents": [ 3040, 5762, 23336 ], "type_id": 0, "properties": { "xrefs": [ "DOID:0060123", "MEDGEN:83866", "NCIT:C53684", "UMLS:C0347481" ], "synonyms": [ "benign connective and soft tissue neoplasm", "benign connective and soft tissue tumor", "benign connective and soft tissue tumour", "benign mesenchymal cell neoplasm", "benign neoplasm of the soft tissue and bone", "benign tumor of the soft tissue and bone", "benign tumour of the soft tissue and bone", "connective and soft tissue neoplasm, benign", "connective tissue benign neoplasm", "neoplasm of soft tissue", "neoplasm of soft tissues", "soft tissue benign neoplasm", "tumor of the soft tissue", "tumour of the soft tissue" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" } ], "definition": "A non-metastasizing neoplasm that arises from the connective and soft tissue. Representative examples include lipoma, leiomyoma, fibroma, and osteoma." }, "child_count": 15, "reference_id": "MONDO:0000654" }, { "id": 18958, "label": "bone neoplasm", "isLeaf": false, "isRoot": false, "parents": [ 7061, 20678 ], "type_id": 0, "properties": { "xrefs": [ "EFO:0003820", "GARD:0018892", "ICD10CM:C40-C41", "MEDGEN:488993", "NCIT:C9343", "ONCOTREE:BONE", "Orphanet:68411", "UMLS:C2732838" ], "synonyms": [ "bone neoplasm", "bone neoplasms", "bone tissue neoplasm", "bone tissue tumor", "bone tissue tumour", "bone tumor", "bone tumors", "bone tumour", "bone tumours", "neoplasm of bone", "neoplasm of bone tissue", "neoplasm of the bone", "osseous neoplasm", "osseous tumor", "osseous tumour", "tumor of bone", "tumor of bone tissue", "tumor of the bone", "tumour of bone", "tumour of bone tissue", "tumour of the bone", "primary bone cancer", "primary malignant neoplasm of bone", "rare bone tumor", "rare bone tumour" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" } ], "definition": "A benign, intermediate, or malignant neoplasm involving the bone or articular cartilage." }, "child_count": 40, "reference_id": "MONDO:0019060" } ], "children": [ { "id": 2964, "label": "bone ameloblastoma", "isLeaf": true, "isRoot": false, "parents": [ 3036, 18018 ], "type_id": 0, "properties": { "xrefs": [ "DOID:0050895", "GARD:0022782" ], "synonyms": [ "ameloblastoma of bone tissue", "bone tissue ameloblastoma" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" }, { "ref": "MONDO:0006858", "name": "mouth disorder" } ], "definition": "A ameloblastoma that involves the bone tissue." }, "child_count": 0, "reference_id": "MONDO:0000513" }, { "id": 2967, "label": "phalanx chondroma", "isLeaf": true, "isRoot": false, "parents": [ 3036, 4459 ], "type_id": 0, "properties": { "xrefs": [ "DOID:0050898", "GARD:0022785" ], "synonyms": [ "phalanx chondroma" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" } ], "definition": "A chondroma that involves the phalanx." }, "child_count": 0, "reference_id": "MONDO:0000516" }, { "id": 4254, "label": "ossifying fibroma", "isLeaf": false, "isRoot": false, "parents": [ 3036 ], "type_id": 0, "properties": { "xrefs": [ "DOID:180", "GARD:0012792", "HP:0030426", "ICDO:9262/0", "ICDO:9274/0", "MEDGEN:104906", "MESH:D018214", "NCIT:C173820", "NCIT:C8422", "NORD:111729", "UMLS:C0206640" ], "synonyms": [ "Cementifying fibroma", "cemento-ossifying fibroma", "fibroma, ossifying, benign", "ossifying fibroma", "ossifying fibroma (disease)", "Juvenile Ossifying Fibroma", "juvenile ossifying fibroma" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" } ], "definition": "A well circumscribed lesion of the bone, most frequently arising from the posterior mandible. It is characterized by the presence of fibrous tissue and a mineralized component which may be woven bone, lamellar bone, or cementum-like material. Complete removal is recommended, since it continues to enlarge if left untreated." }, "child_count": 1, "reference_id": "MONDO:0002119" }, { "id": 4458, "label": "periosteal chondroma", "isLeaf": true, "isRoot": false, "parents": [ 3036, 4459 ], "type_id": 0, "properties": { "xrefs": [ "DOID:2601", "GARD:0023124", "ICDO:9221/0", "MEDGEN:87260", "NCIT:C4302", "UMLS:C0334548" ], "synonyms": [ "juxtacortical chondroma", "juxtacortical chondroma (morphologic abnormality)", "periosteal chondroma" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" } ], "definition": "A benign neoplasm of bone surface composed of hyaline cartilage. It arises beneath the periosteum and is characterized by the presence of chondrocytes, a lobulated growth pattern, and calcification." }, "child_count": 0, "reference_id": "MONDO:0002359" }, { "id": 6738, "label": "chondroblastoma", "isLeaf": true, "isRoot": false, "parents": [ 3036, 21426 ], "type_id": 0, "properties": { "xrefs": [ "DOID:2649", "EFO:0000331", "GARD:0006047", "HP:0030432", "ICDO:9230/0", "MEDGEN:40270", "MESH:D002804", "NANDO:2200051", "NCIT:C2945", "ONCOTREE:CHBL", "UMLS:C0008441" ], "synonyms": [ "chondroblastoma", "chondroblastoma (disease)", "CHBL" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" } ], "definition": "A benign, chondroid-producing, well-circumscribed, lytic neoplasm usually arising from the epiphysis of long bones. It is characterized by the presence of chondroblasts, osteoclast-like giant cells, chondroid formation, calcification, and mitotic activity. In aggressive cases, there is rearrangement of the 8q21 chromosome band. It occurs most frequently in children and young adults and rarely metastasizes." }, "child_count": 0, "reference_id": "MONDO:0004997" }, { "id": 6888, "label": "osteoma", "isLeaf": false, "isRoot": false, "parents": [ 3036 ], "type_id": 0, "properties": { "xrefs": [ "EFO:0002423", "GARD:0024158", "HP:0100246", "ICDO:9180/0", "MEDGEN:18220", "MESH:D010016", "NCIT:C3296", "SCTID:302858007", "UMLS:C0029440" ], "synonyms": [ "osteoma", "osteoma (disease)", "osteoma, benign" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" } ], "definition": "A benign, well-circumscribed, bone-forming neoplasm predominantly composed of lamellar bone. It usually arises from the calvarial, facial, or jaw bones. It is usually asymptomatic but it may cause local swelling or obstruction of the paranasal sinuses. Asymptomatic cases have an indolent clinical course." }, "child_count": 1, "reference_id": "MONDO:0005166" }, { "id": 7879, "label": "paranasal sinus Schneiderian papilloma", "isLeaf": false, "isRoot": false, "parents": [ 2881, 3036, 3038, 6984, 20319 ], "type_id": 0, "properties": { "xrefs": [ "GARD:0024380", "MEDGEN:235462", "NCIT:C6835", "UMLS:C1335343" ], "synonyms": [ "paranasal sinus Schneiderian papilloma", "Schneiderian papilloma of accessory sinus", "Schneiderian papilloma of paranasal sinus", "Schneiderian papilloma of the accessory sinus", "Schneiderian papilloma of the paranasal sinus", "accessory sinus Schneiderian papilloma" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" }, { "ref": "MONDO:0005071", "name": "nervous system disorder" }, { "ref": "MONDO:0005087", "name": "respiratory system disorder" }, { "ref": "MONDO:0024623", "name": "otorhinolaryngologic disease" } ], "definition": "A papilloma that arises from the ciliated respiratory mucosa that lines the paranasal sinuses. It is classified as inverted papilloma and oncocytic papilloma." }, "child_count": 20, "reference_id": "MONDO:0006353" }, { "id": 11017, "label": "osteoid osteoma", "isLeaf": true, "isRoot": false, "parents": [ 3036, 23538 ], "type_id": 0, "properties": { "xrefs": [ "GARD:0024697", "HP:0030433", "ICDO:9191/0", "MEDGEN:18221", "MESH:D010017", "NCIT:C3297", "OMIM:259550", "SCTID:302859004", "UMLS:C0029441" ], "synonyms": [ "osteoid osteoma", "osteoid osteoma (disease)" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" } ], "definition": "A small, benign, bone-forming neoplasm that can arise from any bone but more frequently affects the long bones. The central portion of the neoplasm (nidus) contains differentiated osteoblasts which produce osteoid and sometimes bone. The lesion is usually surrounded by hypervascular sclerotic bone and has limited growth potential. Clinical signs and symptoms include pain and localized tenderness, at the site of the lesion. The pain may be intense but in the majority of cases it is completely alleviated by non-steroidal anti-inflammatory drugs. Prognosis is excellent and recurrences are rare." }, "child_count": 0, "reference_id": "MONDO:0009808" }, { "id": 11768, "label": "CHILD syndrome", "isLeaf": true, "isRoot": false, "parents": [ 3036, 6801, 16089, 16607, 17598, 19104, 19476, 21247, 23867 ], "type_id": 0, "properties": { "xrefs": [ "DOID:0111822", "GARD:0006039", "ICD9:759.89", "MEDGEN:82697", "MESH:C562515", "NANDO:1200629", "NANDO:2200998", "NANDO:2201358", "NORD:1284", "OMIM:308050", "Orphanet:139", "SCTID:17608003", "UMLS:C0265267" ], "synonyms": [ "CHILD syndrome", "CHILD syndrome, X-linked dominant", "Ichthyosis, CHILD Syndrome", "child nevus", "child syndrome", "congenital hemidysplasia with ichthyosiform erythroderma and limb defects", "congenital hemidysplasia with ichthyosiform nevus and limb defects", "ichthyosiform erythroderma, unilateral, with ipsilateral malformations, especially absence deformity of limbs", "ichthyosis, child syndrome" ], "categories": [ { "ref": "MONDO:0002051", "name": "integumentary system disorder" }, { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0002254", "name": "syndromic disease" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" } ], "definition": "CHILD syndrome (Congenital Hemidysplasia with Ichthyosiform nevus and Limb Defects, CS) is an X-linked dominant genodermatosis characterized by unilateral inflammatory and scaling skin lesions with ipsilateral visceral and limb anomalies." }, "child_count": 0, "reference_id": "MONDO:0010621" }, { "id": 18493, "label": "chondromyxoid fibroma", "isLeaf": true, "isRoot": false, "parents": [ 3036, 21426 ], "type_id": 0, "properties": { "xrefs": [ "EFO:0000332", "GARD:0021720", "ICDO:9241/0", "MEDGEN:66375", "NCIT:C3830", "Orphanet:404507", "UMLS:C0221290" ], "synonyms": [ "Chondromyxoid fibroma" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" } ], "definition": "An uncommon benign cartilaginous neoplasm arising from the bone. It is characterized by the presence of spindle-shaped or stellate chondrocytes, a lobulated growth pattern, myxoid stroma formation, and sometimes multinucleated giant cells. It has been associated with chromosomal rearrangement of 6q13 and 6q25 bands. The most common clinical symptom is mild, localized pain." }, "child_count": 0, "reference_id": "MONDO:0018447" }, { "id": 18835, "label": "craniopharyngioma", "isLeaf": false, "isRoot": false, "parents": [ 3033, 3036, 4600, 4759, 21213, 22952 ], "type_id": 0, "properties": { "xrefs": [ "DOID:3840", "EFO:1000209", "GARD:0010486", "ICD9:237.0", "ICDO:9350/1", "MEDGEN:41339", "MESH:D003397", "MedDRA:10011318", "NANDO:2200091", "NCIT:C2964", "NORD:1996", "Orphanet:54595", "SCTID:189179009", "UMLS:C0010276" ], "synonyms": [ "Rathke pouch neoplasm", "Rathke pouch tumor", "Rathke pouch tumour", "Rathke's pouch neoplasm", "Rathke's pouch tumor", "Rathke's pouch tumour", "craniopharyngioma (WHO grade I)", "craniopharyngioma (morphologic abnormality)", "craniopharyngioma, benign", "neoplasm of Rathke's pouch", "tumor of Rathke's pouch", "tumour of Rathke's pouch", "Adamantinomatous tumor", "Adamantinomatous tumour", "Dysodontogenic epithelial tumor", "Dysodontogenic epithelial tumour", "craniopharyngeal duct tumor", "craniopharyngeal duct tumour", "cystoma" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" }, { "ref": "MONDO:0005071", "name": "nervous system disorder" } ], "definition": "A benign, partly cystic, epithelial tumor of the sellar region, presumably derived from Rathke pouch epithelium. It affects mainly children and young adults. There are two clinicopathological forms: adamantinomatous craniopharyngioma and papillary craniopharyngioma. The most significant factor associated with recurrence is the extent of surgical resection, with lesions greater than 5 cm in diameter carrying a markedly worse prognosis. (Adapted from WHO)" }, "child_count": 12, "reference_id": "MONDO:0018907" }, { "id": 18858, "label": "osteoblastoma", "isLeaf": true, "isRoot": false, "parents": [ 3036 ], "type_id": 0, "properties": { "xrefs": [ "DOID:0060098", "GARD:0018854", "HP:0011846", "ICDO:9200/0", "MEDGEN:18212", "MESH:D018215", "MedDRA:10004430", "NCIT:C3294", "Orphanet:58040", "UMLS:C0029417", "icd11.foundation:1948326341" ], "synonyms": [ "giant osteoid osteoma", "ossifying giant cell tumor", "ossifying giant cell tumour", "osteoblastoma", "osteoblastoma (disease)", "osteoblastoma, benign" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" } ], "definition": "A rare benign bone-forming neoplasm usually arising from the spine. It is a well-circumscribed lytic tumor that varies in size. The tumor is composed of woven bone trabeculae and shares similar histologic characteristics with the osteoid osteoma. Surgical curettage is the treatment of choice. The prognosis is excellent." }, "child_count": 0, "reference_id": "MONDO:0018936" }, { "id": 20563, "label": "benign neoplasm of pituitary gland", "isLeaf": true, "isRoot": false, "parents": [ 2882, 3032, 3036, 17888, 20573 ], "type_id": 0, "properties": { "xrefs": [ "DOID:60009", "GARD:0025319", "ICD10CM:D35.2", "MEDGEN:141679", "NCIT:C4782", "SCTID:92296004", "UMLS:C0496901", "icd11.foundation:1871539651" ], "synonyms": [ "benign neoplasm of pituitary", "benign neoplasm of the pituitary", "benign neoplasm of the pituitary gland", "benign pituitary gland neoplasm", "benign pituitary gland tumor", "benign pituitary gland tumour", "benign pituitary neoplasm", "benign pituitary tumor", "benign pituitary tumour", "benign tumor of pituitary", "benign tumor of pituitary gland", "benign tumor of the pituitary", "benign tumor of the pituitary gland", "benign tumour of pituitary", "benign tumour of pituitary gland", "benign tumour of the pituitary", "benign tumour of the pituitary gland", "pituitary gland benign neoplasm", "pituitary neoplasms, benign", "pituitary tumor, benign" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" }, { "ref": "MONDO:0005039", "name": "reproductive system disorder" }, { "ref": "MONDO:0005071", "name": "nervous system disorder" }, { "ref": "MONDO:0005151", "name": "endocrine system disorder" } ], "definition": "A benign neoplasm that involves the pituitary gland." }, "child_count": 0, "reference_id": "MONDO:0021439" }, { "id": 20598, "label": "benign neoplasm of sphenoidal sinus", "isLeaf": false, "isRoot": false, "parents": [ 2881, 3036, 3038, 5888 ], "type_id": 0, "properties": { "xrefs": [ "GARD:0025322", "ICD9:212.0", "MEDGEN:83387", "NCIT:C4422", "SCTID:92404006", "UMLS:C0345678" ], "synonyms": [ "benign neoplasm of sphenoid sinus", "benign neoplasm of the sphenoid sinus", "benign neoplasm of the sphenoidal sinus", "benign sphenoid sinus neoplasm", "benign sphenoid sinus tumor", "benign sphenoid sinus tumour", "benign sphenoidal sinus neoplasm", "benign sphenoidal sinus tumor", "benign sphenoidal sinus tumour", "benign tumor of sphenoid sinus", "benign tumor of sphenoidal sinus", "benign tumor of the sphenoid sinus", "benign tumor of the sphenoidal sinus", "benign tumour of sphenoid sinus", "benign tumour of sphenoidal sinus", "benign tumour of the sphenoid sinus", "benign tumour of the sphenoidal sinus", "sphenoidal sinus benign neoplasm" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" }, { "ref": "MONDO:0005071", "name": "nervous system disorder" }, { "ref": "MONDO:0005087", "name": "respiratory system disorder" }, { "ref": "MONDO:0024623", "name": "otorhinolaryngologic disease" } ], "definition": "A non-metastasizing neoplasm that arises from the sphenoid sinus." }, "child_count": 4, "reference_id": "MONDO:0021477" }, { "id": 20604, "label": "benign neoplasm of frontal sinus", "isLeaf": false, "isRoot": false, "parents": [ 2881, 3036, 3038, 3942 ], "type_id": 0, "properties": { "xrefs": [ "GARD:0025323", "ICD9:212.0", "MEDGEN:87510", "NCIT:C4420", "SCTID:92115005", "UMLS:C0345674", "icd11.foundation:399551439" ], "synonyms": [ "benign frontal sinus neoplasm", "benign frontal sinus tumor", "benign frontal sinus tumour", "benign neoplasm of the frontal sinus", "benign tumor of frontal sinus", "benign tumor of the frontal sinus", "benign tumour of frontal sinus", "benign tumour of the frontal sinus", "frontal sinus benign neoplasm" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" }, { "ref": "MONDO:0005071", "name": "nervous system disorder" }, { "ref": "MONDO:0005087", "name": "respiratory system disorder" }, { "ref": "MONDO:0024623", "name": "otorhinolaryngologic disease" } ], "definition": "A benign neoplasm that involves the frontal sinus." }, "child_count": 4, "reference_id": "MONDO:0021483" }, { "id": 20605, "label": "benign neoplasm of maxillary sinus", "isLeaf": false, "isRoot": false, "parents": [ 2881, 3036, 3038, 8294 ], "type_id": 0, "properties": { "xrefs": [ "GARD:0025324", "ICD9:212.0", "MEDGEN:138024", "NCIT:C4414", "SCTID:92211008", "UMLS:C0345666", "icd11.foundation:1738455612" ], "synonyms": [ "benign maxillary antrum neoplasm", "benign maxillary antrum tumor", "benign maxillary antrum tumour", "benign maxillary sinus neoplasm", "benign maxillary sinus tumor", "benign maxillary sinus tumour", "benign maxillofacial sinus neoplasm", "benign maxillofacial sinus tumor", "benign maxillofacial sinus tumour", "benign neoplasm of maxillary antrum", "benign neoplasm of maxillofacial sinus", "benign neoplasm of the maxillary antrum", "benign neoplasm of the maxillary sinus", "benign neoplasm of the maxillofacial sinus", "benign tumor of maxillary antrum", "benign tumor of maxillary sinus", "benign tumor of maxillofacial sinus", "benign tumor of the maxillary antrum", "benign tumor of the maxillary sinus", "benign tumor of the maxillofacial sinus", "benign tumour of maxillary antrum", "benign tumour of maxillary sinus", "benign tumour of maxillofacial sinus", "benign tumour of the maxillary antrum", "benign tumour of the maxillary sinus", "benign tumour of the maxillofacial sinus", "maxillary sinus benign neoplasm" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" }, { "ref": "MONDO:0005071", "name": "nervous system disorder" }, { "ref": "MONDO:0005087", "name": "respiratory system disorder" }, { "ref": "MONDO:0006858", "name": "mouth disorder" }, { "ref": "MONDO:0024623", "name": "otorhinolaryngologic disease" } ], "definition": "A benign neoplasm that involves the maxillary sinus." }, "child_count": 4, "reference_id": "MONDO:0021484" }, { "id": 20634, "label": "benign neoplasm of ethmoidal sinus", "isLeaf": false, "isRoot": false, "parents": [ 2881, 3036, 3038, 3948 ], "type_id": 0, "properties": { "xrefs": [ "GARD:0025328", "ICD9:212.0", "MEDGEN:91050", "NCIT:C4417", "SCTID:92093000", "UMLS:C0345670" ], "synonyms": [ "benign ethmoid sinus neoplasm", "benign ethmoid sinus tumor", "benign ethmoid sinus tumour", "benign ethmoidal sinus neoplasm", "benign ethmoidal sinus tumor", "benign ethmoidal sinus tumour", "benign neoplasm of ethmoid sinus", "benign neoplasm of the ethmoid sinus", "benign neoplasm of the ethmoidal sinus", "benign tumor of ethmoid sinus", "benign tumor of ethmoidal sinus", "benign tumor of the ethmoid sinus", "benign tumor of the ethmoidal sinus", "benign tumour of ethmoid sinus", "benign tumour of ethmoidal sinus", "benign tumour of the ethmoid sinus", "benign tumour of the ethmoidal sinus", "ethmoid sinus benign neoplasm" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" }, { "ref": "MONDO:0005071", "name": "nervous system disorder" }, { "ref": "MONDO:0005087", "name": "respiratory system disorder" }, { "ref": "MONDO:0024623", "name": "otorhinolaryngologic disease" } ], "definition": "A benign neoplasm that involves the ethmoid sinus." }, "child_count": 4, "reference_id": "MONDO:0021515" }, { "id": 20640, "label": "benign neoplasm of lower jaw bone", "isLeaf": false, "isRoot": false, "parents": [ 3036, 20677 ], "type_id": 0, "properties": { "xrefs": [ "GARD:0025329", "ICD10CM:D16.5", "ICD9:213.1", "MEDGEN:2572", "NCIT:C34417", "SCTID:92208007", "UMLS:C0004994" ], "synonyms": [ "bone of lower jaw benign neoplasm" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" }, { "ref": "MONDO:0006858", "name": "mouth disorder" } ], "definition": "A benign neoplasm that involves the bone of lower jaw." }, "child_count": 2, "reference_id": "MONDO:0021522" }, { "id": 24686, "label": "desmoplastic fibroma", "isLeaf": true, "isRoot": false, "parents": [ 3036 ], "type_id": 0, "properties": { "xrefs": [ "GARD:0027382", "MEDGEN:60200", "UMLS:C0206645" ], "categories": [ { "ref": "MONDO:0002081", "name": "musculoskeletal system disorder" }, { "ref": "MONDO:0003900", "name": "connective tissue disorder" } ] }, "child_count": 0, "reference_id": "MONDO:0700292" } ], "roots": [ { "id": 3054, "label": "benign connective and soft tissue neoplasm" }, { "id": 18958, "label": "bone neoplasm" } ] }