Bilateral coxa valga
Symptom Information:
Symptom ID: | HPO:0010665 | ||||||
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 appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the lower limb(HPO:0002814) Abnormality of the femur(HPO:0002823) Abnormality of the femoral neck or head region(HPO:0003366) Abnormality of the femoral neck(HPO:0003367) Coxa valga(HPO:0002673) Bilateral coxa valga(HPO:0010665) MedDRA: |
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Database Frequency: | 4 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
48,XXYY syndrome | (Orphanet:10) |
RIENHOFF SYNDROME | (OMIM:615582) |
Steinert myotonic dystrophy | (Orphanet:273) |
Wolcott-Rallison syndrome | (Orphanet:1667) |