Osteolysis
Symptom Information:
Symptom ID: | HPO:0002797 | ||||||||||||
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) Abnormal bone structure(HPO:0003330) Osteolysis(HPO:0002797) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Bone disorders (excl congenital and fractures)(MedDRA:10005959) Metabolic bone disorders(MedDRA:10027425) Osteolysis(HPO:0002797) |
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Database Frequency: | 68 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Acroosteolysis, dominant type | (Orphanet:955) |
Adamantinoma | (Orphanet:55881) |
Alveolar echinococcosis | (Orphanet:284) |
Autosomal recessive distal osteolysis syndrome | (Orphanet:2776) |
Chronic recurrent multifocal osteomyelitis | (Orphanet:324964) |
Congenital erythropoietic porphyria | (Orphanet:79277) |
Deafness - onychodystrophy | (Orphanet:3231) |
Dermato-cardio-skeletal syndrome, Borrone type | (Orphanet:1266) |
Dermatoosteolysis, Kirghizian type | (Orphanet:1657) |
Desmoid tumor | (Orphanet:873) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Encephalocraniocutaneous lipomatosis | (Orphanet:2396) |
Enchondromatosis | (Orphanet:296) |
Eosinophilic granuloma | (Orphanet:99871) |
Erdheim-Chester disease | (Orphanet:35687) |
Familial dysautonomia | (Orphanet:1764) |
Familial expansile osteolysis | (Orphanet:85195) |
Felty syndrome | (Orphanet:47612) |
Gamma heavy-chain disease | (Orphanet:100026) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Gorlin syndrome | (Orphanet:377) |
Haim-Munk syndrome | (Orphanet:2342) |
Hand-Schüller-Christian disease | (Orphanet:99873) |
Hashimoto-Pritzker syndrome | (Orphanet:99872) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hereditary sensory and autonomic neuropathy type 2 | (Orphanet:970) |
Hodgkin lymphoma, classical | (Orphanet:391) |
Hutchinson-Gilford progeria syndrome | (Orphanet:740) |
Hydatidosis | (Orphanet:400) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Incontinentia pigmenti | (Orphanet:464) |
Infantile myofibromatosis | (Orphanet:2591) |
Intellectual deficit - cataracts - calcified pinnae - myopathy | (Orphanet:3042) |
Juvenile hyaline fibromatosis | (Orphanet:2028) |
KID syndrome | (Orphanet:477) |
Keratoderma hereditarium mutilans | (Orphanet:494) |
Maffucci syndrome | (Orphanet:163634) |
Mal de Meleda | (Orphanet:87503) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
Mixed connective tissue disease | (Orphanet:809) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Mu heavy-chain disease | (Orphanet:100024) |
Multicentric carpo-tarsal osteolysis with or without nephropathy | (Orphanet:2774) |
Multiple osteochondromas | (Orphanet:321) |
Mutilating palmoplantar keratoderma with periorificial keratotic plaques | (Orphanet:659) |
Occipital horn syndrome | (Orphanet:198) |
PAGET DISEASE OF BONE | (OMIM:602080) |
Pachydermoperiostosis | (Orphanet:2796) |
Papillon-Lefèvre syndrome | (Orphanet:678) |
Polyarteritis nodosa | (Orphanet:767) |
Pycnodysostosis | (Orphanet:763) |
Ramon syndrome | (Orphanet:3019) |
Relapsing polychondritis | (Orphanet:728) |
SAPHO syndrome | (Orphanet:793) |
SATOYOSHI SYNDROME | (OMIM:600705) |
Sarcoidosis | (Orphanet:797) |
Scleroderma | (Orphanet:801) |
Systemic mastocytosis | (Orphanet:2467) |
Talo-patello-scaphoid osteolysis | (Orphanet:50809) |
Torg-Winchester syndrome | (Orphanet:3460) |
Xanthoma disseminatum | (Orphanet:158003) |
Zunich-Kaye syndrome | (Orphanet:3474) |