Arthralgia
Symptom Information:
Symptom ID: | HPO:0002829 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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 morphology(HPO:0011842) Abnormal joint morphology(HPO:0001367) Arthralgia(HPO:0002829) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Joint disorders(MedDRA:10023213) Joint related signs and symptoms(MedDRA:10023226) Arthralgia(HPO:0002829) |
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Database Frequency: | 79 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III | (OMIM:615559) |
AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS | (OMIM:616050) |
Adiposis dolorosa | (Orphanet:36397) |
Alkaptonuria | (Orphanet:56) |
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation | (Orphanet:324530) |
Autosomal dominant spastic paraplegia type 8 | (Orphanet:100989) |
Buschke-Ollendorff syndrome | (Orphanet:1306) |
CANDLE syndrome | (Orphanet:325004) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
CHILBLAIN LUPUS 1 | (OMIM:610448) |
CHST3-related skeletal dysplasia | (Orphanet:263463) |
COMPLEMENT COMPONENT C1r/C1s DEFICIENCY | (OMIM:216950) |
CREST syndrome | (Orphanet:90290) |
Carney complex | (Orphanet:1359) |
Chilblain lupus | (Orphanet:90280) |
Cranio-osteoarthropathy | (Orphanet:1525) |
Czech dysplasia, metatarsal type | (Orphanet:137678) |
Dermatoosteolysis, Kirghizian type | (Orphanet:1657) |
Diffuse cutaneous systemic sclerosis | (Orphanet:220393) |
EPIPHYSEAL DYSPLASIA, MULTIPLE, 6 | (OMIM:614135) |
Ehlers-Danlos syndrome due to tenascin-X deficiency | (Orphanet:230839) |
FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 4 | (OMIM:616115) |
FAMILIAL MEDITERRANEAN FEVER | (OMIM:249100) |
FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT | (OMIM:134610) |
Fabry disease | (Orphanet:324) |
Familial Mediterranean fever | (Orphanet:342) |
Familial cold urticaria | (Orphanet:47045) |
HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2 | (OMIM:614441) |
Hemochromatosis type 2 | (Orphanet:79230) |
Hemochromatosis type 3 | (Orphanet:225123) |
Hemochromatosis type 4 | (Orphanet:139491) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hemochromatosis, type 2B | (OMIM:613313) |
Hereditary arterial and articular multiple calcification syndrome | (Orphanet:289601) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hyperimmunoglobulinemia D with periodic fever | (Orphanet:343) |
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1 | (OMIM:161950) |
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2 | (OMIM:613944) |
JMP syndrome | (Orphanet:324999) |
Kniest dysplasia | (Orphanet:485) |
Limited cutaneous systemic sclerosis | (Orphanet:220402) |
MUCOLIPIDOSIS III GAMMA | (OMIM:252605) |
Mediterranean macrothrombocytopenia | (Orphanet:101022) |
Mevalonic aciduria | (Orphanet:29) |
Muckle-Wells syndrome | (Orphanet:575) |
Multicentric carpo-tarsal osteolysis with or without nephropathy | (Orphanet:2774) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Multiple epiphyseal dysplasia type 4 | (Orphanet:93307) |
Multiple epiphyseal dysplasia type 5 | (Orphanet:93311) |
Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia | (Orphanet:166029) |
NLRP12-associated hereditary periodic fever syndrome | (Orphanet:247868) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Non-specific interstitial pneumonia | (Orphanet:91364) |
OSTEOARTHRITIS SUSCEPTIBILITY 3 | (OMIM:607850) |
Otospondylomegaepiphyseal dysplasia | (Orphanet:1427) |
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2 | (OMIM:615399) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Pediatric systemic sclerosis | (Orphanet:93567) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Proteasome disability syndrome | (Orphanet:324977) |
Pseudoachondroplasia | (Orphanet:750) |
Pyle disease | (Orphanet:3005) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED | (OMIM:313400) |
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET | (OMIM:615934) |
SYNOVIAL CHONDROMATOSIS, FAMILIAL, WITH DWARFISM | (OMIM:186575) |
Spondyloepimetaphyseal dysplasia, Irapa type | (Orphanet:93351) |
Sterile multifocal osteomyelitis with periostitis and pustulosis | (Orphanet:210115) |
Stickler syndrome type 3 | (Orphanet:166100) |
TRAPS syndrome | (Orphanet:32960) |
TRICHORHINOPHALANGEAL SYNDROME, TYPE I | (OMIM:190350) |
Torg-Winchester syndrome | (Orphanet:3460) |
Trichorhinophalangeal syndrome type 1 and 3 | (Orphanet:77258) |
Ulna metaphyseal dysplasia syndrome | (Orphanet:1837) |
Upington disease | (Orphanet:3408) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR | (OMIM:600785) |
X-linked hypophosphatemia | (Orphanet:89936) |