Joint hyperflexibility
Symptom Information:
Symptom ID: | HPO:0005692 | |||||||||||||||||
Synonyms: |
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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) Abnormality of joint mobility(HPO:0011729) Joint hypermobility(HPO:0001382) Joint hyperflexibility(HPO:0005692) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Joint disorders(MedDRA:10023213) Joint related disorders NEC(MedDRA:10027685) Joint hyperflexibility(HPO:0005692) |
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Database Frequency: | 20 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
48,XXYY syndrome | (Orphanet:10) |
BRUCK SYNDROME 1 | (OMIM:259450) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE | (OMIM:608763) |
Ehlers-Danlos syndrome, fibronectinemic type | (Orphanet:75501) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Ehlers-Danlos syndrome, spondylocheirodysplastic type | (Orphanet:157965) |
HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES | (OMIM:234800) |
LOEYS-DIETZ SYNDROME 4 | (OMIM:614816) |
LOEYS-DIETZ SYNDROME, TYPE 2A | (OMIM:608967) |
Larsen-like osseous dysplasia - short stature | (Orphanet:2370) |
Menkes disease | (Orphanet:565) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
OSTEOGENESIS IMPERFECTA, TYPE XIII | (OMIM:614856) |
Peters-plus syndrome | (Orphanet:709) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
WARBURG MICRO SYNDROME 1 | (OMIM:600118) |
Wilson disease | (Orphanet:905) |