Exostoses
Symptom Information:
Symptom ID: | HPO:0100777 | |||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |