Joint hyperflexibility

Symptom Information:

Symptom ID: HPO:0005692
Synonyms:
Joint hypermobility [Orphanet:46360]
Joint laxity (finding) [Orphanet:46360]
Range of joint movement increased (finding) [Orphanet:46360]
Hypermobility, Joint [Orphanet:46360]
Joint hyperflexibility [OMIM:Joint hyperflexibility]
Hyperextensible joints/articular hyperlaxity [Orphanet:46360]
Joint laxity [Orphanet:46360]
Joint laxity [MedDRA:10070874]
Joint hypermobility (in some patients) [OMIM:Joint hypermobility (in some patients)]
Joint hypermobility (large and small joints) [OMIM:Joint hypermobility (large and small joints)]
Joint hypermobility (rare) [OMIM:Joint hypermobility (rare)]
Joint laxity (elbow) [OMIM:Joint laxity (elbow)]
Joint laxity (elbow, wrist, fingers) [OMIM:Joint laxity (elbow, wrist, fingers)]
Joint laxity (except elbow) [OMIM:Joint laxity (except elbow)]
Joint laxity (fingers and wrist) [OMIM:Joint laxity (fingers and wrist)]
Joint laxity (hands and feet) [OMIM:Joint laxity (hands and feet)]
Joint laxity (hip, knee, shoulder, wrist, fingers) [OMIM:Joint laxity (hip, knee, shoulder, wrist, fingers)]
Quality:
Cross references:
HPO:0001382 "Joint hypermobility" [Orphanet:46360]
HPO:0001388 "Joint laxity" [Orphanet:46360]
Orphanet:46360 "Hyperextensible joints/articular hyperlaxity" [Orphanet:46360]
OMIM: "Joint hyperflexibility" [OMIM:Joint hyperflexibility]
OMIM: "Joint hypermobility (in some patients)" [OMIM:Joint hypermobility (in some patients)]
OMIM: "Joint hypermobility (large and small joints)" [OMIM:Joint hypermobility (large and small joints)]
OMIM: "Joint hypermobility (rare)" [OMIM:Joint hypermobility (rare)]
OMIM: "Joint laxity (elbow)" [OMIM:Joint laxity (elbow)]
OMIM: "Joint laxity (elbow, wrist, fingers)" [OMIM:Joint laxity (elbow, wrist, fingers)]
OMIM: "Joint laxity (except elbow)" [OMIM:Joint laxity (except elbow)]
OMIM: "Joint laxity (fingers and wrist)" [OMIM:Joint laxity (fingers and wrist)]
OMIM: "Joint laxity (hands and feet)" [OMIM:Joint laxity (hands and feet)]
OMIM: "Joint laxity (hip, knee, shoulder, wrist, fingers)" [OMIM:Joint laxity (hip, knee, shoulder, wrist, fingers)]
UMLS:C0086437 "Hypermobility, Joint" [Orphanet:46360]
Is a (Direct Parents):
HPO         Joint hypermobility
Orphanet Abnormal cartilage morphology
MedDRA Joint related disorders NEC
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)
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)