Bone pain
Symptom Information:
Symptom ID: | HPO:0002653 | ||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||
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) Bone pain(HPO:0002653) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Bone disorders (excl congenital and fractures)(MedDRA:10005959) Bone related signs and symptoms(MedDRA:10006006) Bone pain(HPO:0002653) |
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Database Frequency: | 75 / 7739 | ||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acroosteolysis, dominant type | (Orphanet:955) |
Adamantinoma | (Orphanet:55881) |
Adult hypophosphatasia | (Orphanet:247676) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Albers-Schönberg osteopetrosis | (Orphanet:53) |
Angio-osteohypertrophic syndrome | (Orphanet:2346) |
Atypical Gaucher disease due to saposin C deficiency | (Orphanet:309252) |
Autosomal dominant hypophosphatemic rickets | (Orphanet:89937) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
BONE PAIN, PERIODIC | (OMIM:112270) |
Blue rubber bleb nevus | (Orphanet:1059) |
Buschke-Ollendorff syndrome | (Orphanet:1306) |
CANDLE syndrome | (Orphanet:325004) |
Camurati-Engelmann disease | (Orphanet:1328) |
Cholestasis - lymphedema | (Orphanet:1414) |
Chronic recurrent multifocal osteomyelitis | (Orphanet:324964) |
Cobb syndrome | (Orphanet:53721) |
Dent disease type 1 | (Orphanet:93622) |
Dermatitis herpetiformis | (Orphanet:1656) |
Dysplasia epiphysealis hemimelica | (Orphanet:1822) |
Enchondromatosis | (Orphanet:296) |
Eosinophilic granuloma | (Orphanet:99871) |
Erdheim-Chester disease | (Orphanet:35687) |
Facial dysmorphism - immunodeficiency - livedo - short stature | (Orphanet:352712) |
Familial expansile osteolysis | (Orphanet:85195) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM | (OMIM:612089) |
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE | (OMIM:300554) |
Hereditary hypophosphatemic rickets with hypercalciuria | (Orphanet:157215) |
Hodgkin lymphoma | (Orphanet:98293) |
Hodgkin lymphoma, classical | (Orphanet:391) |
Hypocalcemic vitamin D-dependent rickets | (Orphanet:289157) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Idiopathic juvenile osteoporosis | (Orphanet:85193) |
JMP syndrome | (Orphanet:324999) |
Kienbock disease | (Orphanet:97332) |
Langer-Giedion syndrome | (Orphanet:502) |
Madelung deformity | (Orphanet:35688) |
Maffucci syndrome | (Orphanet:163634) |
Majeed syndrome | (Orphanet:77297) |
McCune-Albright syndrome | (Orphanet:562) |
Melorheostosis | (Orphanet:2485) |
Metachondromatosis | (Orphanet:2499) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Multiple osteochondromas | (Orphanet:321) |
NEUROBLASTOMA, SUSCEPTIBILITY TONEUROBLASTOMA, SUSCEPTIBILITY TO, 1, INCLUDED | (OMIM:256700) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Nasu-Hakola disease | (Orphanet:2770) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Neuroblastoma | (Orphanet:635) |
Osteopetrosis | (Orphanet:2781) |
Osteopetrosis with renal tubular acidosis | (Orphanet:2785) |
PAGET DISEASE OF BONE | (OMIM:602080) |
PAGET DISEASE OF BONE 1 | (OMIM:167250) |
PAGET DISEASE OF BONE 4 | (OMIM:606263) |
Pachydermoperiostosis | (Orphanet:2796) |
Primary hyperoxaluria | (Orphanet:416) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Progressive non-infectious anterior vertebral fusion | (Orphanet:2062) |
Progressive osseous heteroplasia | (Orphanet:2762) |
Proteasome disability syndrome | (Orphanet:324977) |
Pycnodysostosis | (Orphanet:763) |
SAPHO syndrome | (Orphanet:793) |
Schnitzler syndrome | (Orphanet:37748) |
Stickler syndrome | (Orphanet:828) |
Systemic mastocytosis | (Orphanet:2467) |
Tumoral calcinosis | (Orphanet:53715) |
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A | (OMIM:264700) |
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B | (OMIM:600081) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2A | (OMIM:277440) |
Wilson disease | (Orphanet:905) |
X-linked hypophosphatemia | (Orphanet:89936) |