Osteomyelitis

Symptom Information:

Symptom ID: HPO:0002754
Synonyms:
Osteomyelitis (disorder) [Orphanet:45600]
Osteomyelitis [Orphanet:45600]
Osteomyelitis [OMIM:Osteomyelitis]
Osteomyelitis/osteitis/periostitis/spondylodisciitis [Orphanet:45600]
Osteomyelitis [MedDRA:10031252]
Bone infection NOS [MedDRA:10031252]
Hip osteomyelitis [MedDRA:10031252]
Orbital osteomyelitis [MedDRA:10031252]
Osteomyelitis NOS [MedDRA:10031252]
Osteomyelitis, periostitis, and other infections involving bone [MedDRA:10031252]
Other infections involving bone [MedDRA:10031252]
Other infections involving bone disease classified elsewhere , multiple sites [MedDRA:10031252]
Other infections involving bone disease classified elsewhere, upper arm [MedDRA:10031252]
Other infections involving bone diseases classified elsewhere, ankle and foot [MedDRA:10031252]
Other infections involving bone diseases classified elsewhere, lower leg [MedDRA:10031252]
Other infections involving bone diseases classified elsewhere, other specified sites [MedDRA:10031252]
Other infections involving bone diseases classified elsewhere, pelvic region and thigh [MedDRA:10031252]
Other infections involving bone diseases classified elsewhere, shoulder region [MedDRA:10031252]
Other infections involving bone diseases classified elsewhere, unspecified infection of bone [MedDRA:10031252]
Other infections involving bone in diseases classified elsewhere [MedDRA:10031252]
Other infections involving bone in diseases classified elsewhere, forearm [MedDRA:10031252]
Other infections involving bone in diseases classified elsewhere, site unspecified [MedDRA:10031252]
Other infections involving diseases classified elsewhere, hand bone [MedDRA:10031252]
Unspecified infection of bone [MedDRA:10031252]
Unspecified infection of bone in multiple sites [MedDRA:10031252]
Unspecified infection of bone of other specified sites [MedDRA:10031252]
Unspecified infection of bone of pelvic region and thigh [MedDRA:10031252]
Unspecified infection of bone of shoulder region [MedDRA:10031252]
Unspecified infection of bone, ankle and foot [MedDRA:10031252]
Unspecified infection of bone, forearm [MedDRA:10031252]
Unspecified infection of bone, hand [MedDRA:10031252]
Unspecified infection of bone, lower leg [MedDRA:10031252]
Unspecified infection of bone, site unspecified [MedDRA:10031252]
Unspecified infection of bone, upper arm [MedDRA:10031252]
Unspecified osteomyelitis [MedDRA:10031252]
Unspecified osteomyelitis involving ankle and foot [MedDRA:10031252]
Unspecified osteomyelitis involving forearm [MedDRA:10031252]
Unspecified osteomyelitis involving hand [MedDRA:10031252]
Unspecified osteomyelitis involving lower leg [MedDRA:10031252]
Unspecified osteomyelitis involving multiple sites [MedDRA:10031252]
Unspecified osteomyelitis involving other specified sites [MedDRA:10031252]
Unspecified osteomyelitis involving pelvic region and thigh [MedDRA:10031252]
Unspecified osteomyelitis involving shoulder region [MedDRA:10031252]
Unspecified osteomyelitis involving upper arm [MedDRA:10031252]
Unspecified osteomyelitis, site unspecified [MedDRA:10031252]
Bone infection [MedDRA:10031252]
Spinal osteomyelitis [MedDRA:10031252]
Osteomyelitis of jaw [MedDRA:10031252]
Osteomyelitis aggravated [MedDRA:10031252]
Osteomyelitis recurrent [MedDRA:10031252]
Osteitis [MedDRA:10031149]
Bone inflammatory disease (disorder) [Orphanet:45600]
Osteitis (disorder) [Orphanet:45600]
Osteitis [Orphanet:45600]
Periostitis [MedDRA:10034551]
Periostitis (disorder) [Orphanet:45600]
Periostitis [Orphanet:45600]
Intervertebral discitis [MedDRA:10060738]
Spondylodiscitis [Orphanet:45600]
Discitis (disorder) [Orphanet:45600]
Discitis [Orphanet:45600]
Quality:
Cross references:
Orphanet:45600 "Osteomyelitis/osteitis/periostitis/spondylodisciitis" [Orphanet:45600]
OMIM: "Osteomyelitis" [OMIM:Osteomyelitis]
UMLS:C0029443 "Osteomyelitis" [HPO:0002754]
UMLS:C0029443 "Osteomyelitis" [Orphanet:45600]
UMLS:C0029400 "Osteitis" [Orphanet:45600]
UMLS:C0031111 "Periostitis" [Orphanet:45600]
UMLS:C0012624 "Discitis" [Orphanet:45600]
Is a (Direct Parents):
Orphanet Abnormality of the skeletal system
HPO         Abnormality of skeletal physiology
MedDRA Bone and joint infections (excl arthritis)
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal physiology(HPO:0011843)
             Osteomyelitis(HPO:0002754)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Bone disorders (excl congenital and fractures)(MedDRA:10005959)
       Bone and joint infections (excl arthritis)(MedDRA:10005941)
          Osteomyelitis(HPO:0002754)
Database Frequency: 37 / 7739
Resource:

All diseases associated with this symptom:

Albers-Schönberg osteopetrosis (Orphanet:53)
Autosomal agammaglobulinemia (Orphanet:33110)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Cervical hypertrichosis - peripheral neuropathy (Orphanet:2218)
Chronic recurrent multifocal osteomyelitis (Orphanet:324964)
Cyclic neutropenia (Orphanet:2686)
Erdheim-Chester disease (Orphanet:35687)
FANCONI-LIKE SYNDROME (OMIM:227850)
Gaucher disease (Orphanet:355)
Gaucher disease type 1 (Orphanet:77259)
Gnathodiaphyseal dysplasia (Orphanet:53697)
HEMOGLOBIN--BETA LOCUS (OMIM:141900)
Hashimoto-Pritzker syndrome (Orphanet:99872)
Hereditary sensory and autonomic neuropathy type 1 (Orphanet:36386)
Hereditary sensory and autonomic neuropathy type 4 (Orphanet:642)
Hereditary sensory and autonomic neuropathy with spastic paraplegia (Orphanet:139578)
Hyper-IgM syndrome type 4 (Orphanet:101091)
Intestinal lymphangiectasia (Orphanet:36204)
Majeed syndrome (Orphanet:77297)
Menkes disease (Orphanet:565)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC (OMIM:613640)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB (OMIM:613115)
NEUROPATHY, HEREDITARY SENSORY, TYPE IE (OMIM:614116)
NEUROPATHY, HEREDITARY SENSORY, TYPE IF (OMIM:615632)
Neutropenia, severe congenital, 1, autosomal dominant (OMIM:202700)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1 (OMIM:259700)
Osteopetrosis (Orphanet:2781)
Pachydermoperiostosis (Orphanet:2796)
Polyarteritis nodosa (Orphanet:767)
Pycnodysostosis (Orphanet:763)
Reactive arthritis (Orphanet:29207)
SAPHO syndrome (Orphanet:793)
Scleroderma (Orphanet:801)
Sterile multifocal osteomyelitis with periostitis and pustulosis (Orphanet:210115)
Tumoral calcinosis (Orphanet:53715)
X-linked agammaglobulinemia (Orphanet:47)