Osteolysis

Symptom Information:

Symptom ID: HPO:0002797
Synonyms:
Increased bone resorption [HPO:0002797]
Osteolytic defects of bones [HPO:0002797]
Osteolysis (disorder) [Orphanet:45420]
Osteolysis (morphologic abnormality) [Orphanet:45420]
Osteolysis [Orphanet:45420]
Osteolysis [OMIM:Osteolysis]
Osteolysis/osteoclasia/bone destruction/erosions [Orphanet:45420]
Osteolysis [MedDRA:10031248]
Acroosteolysis [MedDRA:10031248]
Osteolytic lesion [MedDRA:10031248]
Osteolytic lesions [OMIM:Osteolytic lesions]
Resorption bone increased [MedDRA:10038642]
Quality:
Cross references:
Orphanet:45420 "Osteolysis/osteoclasia/bone destruction/erosions" [Orphanet:45420]
OMIM: "Osteolysis" [OMIM:Osteolysis]
OMIM: "Osteolytic lesions" [OMIM:Osteolytic lesions]
UMLS:C0029435 "Osteolysis" [HPO:0002797]
UMLS:C0029435 "Osteolysis" [Orphanet:45420]
Is a (Direct Parents):
HPO         Osteolysis involving bones of the upper limbs
Orphanet Abnormality of the skeletal system
MedDRA Metabolic bone disorders
HPO         Abnormal bone structure
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)
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)