Osteomyelitis
Symptom Information:
Symptom ID: | HPO:0002754 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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 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) |
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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) |