Hyperostosis
Symptom Information:
Symptom ID: | HPO:0100774 | ||||||||||||||||||||
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) 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) |
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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) |