Neoplasm of the skeletal system

Symptom Information:

Symptom ID: HPO:0010622
Neoplasia of the skeletal system [HPO:0010622]
Bone tumor [Orphanet:45690]
Bone tumor (morphologic abnormality) [Orphanet:45690]
Neoplasm of bone (disorder) [Orphanet:45690]
Bone neoplasms [Orphanet:45690]
Bone tumefaction/swelling [Orphanet:45690]
Bone neoplasm [Orphanet:45690]
Bone neoplasm [MedDRA:10005995]
Bone neoplasm NOS [MedDRA:10005995]
Neoplasm bone [MedDRA:10005995]
Neoplasm of uncertain behavior of bone and articular cartilage [MedDRA:10005995]
Neoplasm of uncertain behaviour of bone and articular cartilage [MedDRA:10005995]
Vertebral column neoplasm [MedDRA:10005995]
Neoplasm of maxilla [MedDRA:10005995]
Cross references:
Orphanet:45690 "Bone tumefaction/swelling" [Orphanet:45690]
UMLS:C0005967 "Bone neoplasms" [Orphanet:45690]
Is a (Direct Parents):
HPO         Enchondroma
HPO         Osteochondroma
Orphanet Abnormality of the skeletal system
HPO         Neoplasm by anatomical site
MedDRA Musculoskeletal and connective tissue neoplasms NEC
HPO         Abnormality of skeletal morphology
HPO         Chondroblastoma
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the skeletal system(HPO:0010622)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Neoplasm of the skeletal system(HPO:0010622)
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue neoplasms(MedDRA:10028389)
       Musculoskeletal and connective tissue neoplasms NEC(MedDRA:10028390)
          Neoplasm of the skeletal system(HPO:0010622)
Database Frequency: 30 / 7739

All diseases associated with this symptom:

Adamantinoma (Orphanet:55881)
Aggressive systemic mastocytosis (Orphanet:98850)
Baller-Gerold syndrome (Orphanet:1225)
CINCA syndrome (Orphanet:1451)
Caffey disease (Orphanet:1310)
Cherubism (Orphanet:184)
Cranio-osteoarthropathy (Orphanet:1525)
Dysspondyloenchondromatosis (Orphanet:85198)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Enchondromatosis (Orphanet:296)
Eosinophilic granuloma (Orphanet:99871)
Focal dermal hypoplasia (Orphanet:2092)
Gaucher disease (Orphanet:355)
Gnathodiaphyseal dysplasia (Orphanet:53697)
Infantile myofibromatosis (Orphanet:2591)
Langer-Giedion syndrome (Orphanet:502)
Li-Fraumeni syndrome (Orphanet:524)
Maffucci syndrome (Orphanet:163634)
Majeed syndrome (Orphanet:77297)
Mazabraud syndrome (Orphanet:57782)
Multiple osteochondromas (Orphanet:321)
Nasu-Hakola disease (Orphanet:2770)
Non-polyposis Turcot syndrome (Orphanet:99817)
OSLAM syndrome (Orphanet:2760)
POEMS syndrome (Orphanet:2905)
Pachydermoperiostosis (Orphanet:2796)
Progressive osseous heteroplasia (Orphanet:2762)
SAPHO syndrome (Orphanet:793)
Sturge-Weber syndrome (Orphanet:3205)
Thymoma (Orphanet:99867)