Exostoses

Symptom Information:

Symptom ID: HPO:0100777
Synonyms:
Exostosis [Orphanet:45300]
Osteochondroma (morphologic abnormality) [Orphanet:45300]
Chondroma of bone (disorder) [Orphanet:45300]
External hyperostosis (morphologic abnormality) [Orphanet:45300]
Exostosis (disorder) [Orphanet:45300]
Osteochondroma (disorder) [Orphanet:45300]
External exotoses [Orphanet:45300]
Exostoses [Orphanet:45300]
Cartilaginous exostosis [Orphanet:45300]
Exostoses [OMIM:Exostoses]
Osteochondroma [Orphanet:45300]
Osteochondroma [MedDRA:10059587]
Exostosis [MedDRA:10015688]
Bone hypertrophy [MedDRA:10015688]
Bone spur [MedDRA:10015688]
Calcaneal spur [MedDRA:10015688]
Exostosis of orbit [MedDRA:10015688]
Exostosis of unspecified site [MedDRA:10015688]
Foot exostosis [MedDRA:10015688]
Hyperostosis [MedDRA:10015688]
Hyperostosis of skull [MedDRA:10015688]
Heel exostosis [MedDRA:10015688]
Osteophytosis [MedDRA:10015688]
Vertebral osteophyte [MedDRA:10015688]
Haglund deformity [MedDRA:10015688]
Central osteophyte [MedDRA:10015688]
Exostoses (in patients with larger deletions involving the EXT1 gene) [OMIM:Exostoses (in patients with larger deletions involving the EXT1 gene)]
Osteochondroma [OMIM:Osteochondroma]
Osteochondromas [OMIM:Osteochondromas]
Quality:
Cross references:
Orphanet:45300 "Exostoses" [Orphanet:45300]
OMIM: "Exostoses" [OMIM:Exostoses]
OMIM: "Exostoses (in patients with larger deletions involving the EXT1 gene)" [OMIM:Exostoses (in patients with larger deletions involving the EXT1 gene)]
OMIM: "Osteochondroma" [OMIM:Osteochondroma]
OMIM: "Osteochondromas" [OMIM:Osteochondromas]
UMLS:C0015302 "External exotoses" [Orphanet:45300]
UMLS:C1442903 "Exostoses" [Orphanet:45300]
UMLS:C0029423 "Cartilaginous exostosis" [Orphanet:45300]
Is a (Direct Parents):
MedDRA Bone disorders NEC
MedDRA Cartilage neoplasms benign
HPO         Neoplasm of the skeletal system
Orphanet Abnormality of the skeletal system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Neoplasm of the skeletal system(HPO:0010622)
                Exostoses(HPO:0100777)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the skeletal system(HPO:0010622)
                Exostoses(HPO:0100777)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Bone disorders (excl congenital and fractures)(MedDRA:10005959)
       Bone disorders NEC(MedDRA:10027658)
          Exostoses(HPO:0100777)
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Skeletal neoplasms benign(MedDRA:10040776)
       Cartilage neoplasms benign(MedDRA:10007711)
          Exostoses(HPO:0100777)
Database Frequency: 32 / 7739
Resource:

All diseases associated with this symptom:

8p23.1 microduplication syndrome (Orphanet:251076)
Bazex-Dupré-Christol syndrome (Orphanet:113)
CORNELIA DE LANGE SYNDROME 4 (OMIM:614701)
Camptodactyly - tall stature - scoliosis - hearing loss (Orphanet:85164)
Carpotarsal osteochondromatosis (Orphanet:2767)
Cutis laxa (Orphanet:209)
Dentin dysplasia (Orphanet:1653)
Dysostosis, Stanescu type (Orphanet:1798)
Dysplasia epiphysealis hemimelica (Orphanet:1822)
Dysspondyloenchondromatosis (Orphanet:85198)
EXOSTOSES OF HEEL (OMIM:133600)
Exostoses - anetodermia - brachydactyly type E (Orphanet:1962)
Familial osteochondritis dissecans (Orphanet:251262)
Hypophosphatemic rickets (Orphanet:437)
Langer-Giedion syndrome (Orphanet:502)
Léri-Weill dyschondrosteosis (Orphanet:240)
Madelung deformity (Orphanet:35688)
Maffucci syndrome (Orphanet:163634)
Menkes disease (Orphanet:565)
Metachondromatosis (Orphanet:2499)
Mononen-Karnes-Senac syndrome (Orphanet:2565)
Multiple osteochondromas (Orphanet:321)
Nail-patella syndrome (Orphanet:2614)
Occipital horn syndrome (Orphanet:198)
Oculocerebrocutaneous syndrome (Orphanet:1647)
Potocki-Shaffer syndrome (Orphanet:52022)
Progressive non-infectious anterior vertebral fusion (Orphanet:2062)
Proteus syndrome (Orphanet:744)
Proteus-like syndrome (Orphanet:2969)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Stickler syndrome type 3 (Orphanet:166100)
Upington disease (Orphanet:3408)