Ligamentous laxity
Symptom Information:
Symptom ID: | HPO:0001380 | ||
Synonyms: |
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Quality: | |||
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) Ligamentous laxity(HPO:0001380) MedDRA: |
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Database Frequency: | 8 / 7739 | ||
Resource: |
All diseases associated with this symptom:
AARSKOG SYNDROME, AUTOSOMAL DOMINANT | (OMIM:100050) |
Aarskog-Scott syndrome | (Orphanet:915) |
BARATELA-SCOTT SYNDROME | (OMIM:300881) |
CHROMOSOME 17p13.1 DELETION SYNDROME | (OMIM:613776) |
Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
Larsen-like syndrome, B3GAT3 type | (Orphanet:284139) |
OSTEOGENESIS IMPERFECTA, TYPE VI | (OMIM:613982) |
Pseudoachondroplasia | (Orphanet:750) |