Bone pain

Symptom Information:

Symptom ID: HPO:0002653
Synonyms:
Bone pain (finding) [Orphanet:45630]
Bone pain [Orphanet:45630]
Bone pain [OMIM:Bone pain]
Bone pain [MedDRA:10006002]
Bone pain aggravated [MedDRA:10006002]
Bone swelling painful [MedDRA:10006002]
External tibial bone painful [MedDRA:10006002]
Osteoneuralgia [MedDRA:10006002]
Osteoneurlagia [MedDRA:10006002]
Pain bone [MedDRA:10006002]
Pain femoral [MedDRA:10006002]
Skeletal pain [MedDRA:10006002]
Tibia pain [MedDRA:10006002]
Rachialgia [MedDRA:10006002]
Bone tenderness [MedDRA:10006002]
Ostealgia [MedDRA:10006002]
Bone pain (in some patients) [OMIM:Bone pain (in some patients)]
Bone pain (with metastatic disease) [OMIM:Bone pain (with metastatic disease)]
Quality:
Cross references:
Orphanet:45630 "Bone pain" [Orphanet:45630]
OMIM: "Bone pain" [OMIM:Bone pain]
OMIM: "Bone pain (in some patients)" [OMIM:Bone pain (in some patients)]
OMIM: "Bone pain (with metastatic disease)" [OMIM:Bone pain (with metastatic disease)]
UMLS:C0151825 "Bone pain" [Orphanet:45630]
Is a (Direct Parents):
MedDRA Bone related signs and symptoms
HPO         Abnormality of skeletal physiology
Orphanet Abnormality of the skeletal system
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)
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)