Generalized joint laxity
Symptom Information:
Symptom ID: | HPO:0002761 | |||
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) Abnormality of joint mobility(HPO:0011729) Joint hypermobility(HPO:0001382) Generalized joint laxity(HPO:0002761) MedDRA: |
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Database Frequency: | 8 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Achondroplasia | (Orphanet:15) |
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 | (OMIM:601776) |
Ehlers-Danlos syndrome, musculocontractural type | (Orphanet:2953) |
Hypertryptophanemia | (Orphanet:2224) |
KABUKI SYNDROME 2 | (OMIM:300867) |
Multiple epiphyseal dysplasia type 1 | (Orphanet:93308) |
Multiple epiphyseal dysplasia, with miniepiphyses | (Orphanet:166032) |
OSTEOGENESIS IMPERFECTA, TYPE X | (OMIM:613848) |