Limited hip movement
Symptom Information:
Symptom ID: | HPO:0008800 | ||||
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) Limitation of joint mobility(HPO:0001376) Limited hip movement(HPO:0008800) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of pelvic girdle bone morphology(HPO:0002644) Limited hip movement(HPO:0008800) MedDRA: |
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Database Frequency: | 3 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive omodysplasia | (Orphanet:93329) |
Multiple epiphyseal dysplasia type 1 | (Orphanet:93308) |
Spondyloepiphyseal dysplasia congenita | (Orphanet:94068) |