Hyperostosis

Symptom Information:

Symptom ID: HPO:0100774
Synonyms:
Bone Hypertrophy [HPO:0100774]
Hypertrophy of bone (morphologic abnormality) [Orphanet:45150]
Hypertrophy of bone (disorder) [Orphanet:45150]
Hyperostosis [Orphanet:45150]
Hyperostosis [OMIM:Hyperostosis]
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)]
Quality:
Cross references:
Orphanet:45150 "Hyperostosis" [Orphanet:45150]
OMIM: "Hyperostosis" [OMIM:Hyperostosis]
OMIM: "Exostoses (in patients with larger deletions involving the EXT1 gene)" [OMIM:Exostoses (in patients with larger deletions involving the EXT1 gene)]
UMLS:C0020492 "Hyperostosis" [Orphanet:45150]
Is a (Direct Parents):
Orphanet Abnormality of the skeletal system
HPO         Abnormality of skeletal morphology
MedDRA Bone disorders NEC
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)
             Hyperostosis(HPO:0100774)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Bone disorders (excl congenital and fractures)(MedDRA:10005959)
       Bone disorders NEC(MedDRA:10027658)
          Hyperostosis(HPO:0100774)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

Buschke-Ollendorff syndrome (Orphanet:1306)
CINCA syndrome (Orphanet:1451)
CORNELIA DE LANGE SYNDROME 4 (OMIM:614701)
CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (OMIM:122860)
Camurati-Engelmann disease (Orphanet:1328)
Chronic recurrent multifocal osteomyelitis (Orphanet:324964)
Majeed syndrome (Orphanet:77297)
Melorheostosis (Orphanet:2485)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
Nakajo-Nishimura syndrome (Orphanet:2615)
Oculodentodigital dysplasia (Orphanet:2710)
Proteus syndrome (Orphanet:744)
Proteus-like syndrome (Orphanet:2969)
SAPHO syndrome (Orphanet:793)
Tumoral calcinosis (Orphanet:53715)
Wiskott-Aldrich syndrome (Orphanet:906)