Bilateral coxa valga

Symptom Information:

Symptom ID: HPO:0010665
Synonyms:
Coxa valga [Orphanet:46600]
Hip joint valgus deformity (finding) [Orphanet:46600]
Bilateral coxa valga [OMIM:Bilateral coxa valga]
Hip dislocation/dysplasia/coxa valga/coxa vara/coxa plana [Orphanet:46600]
Quality:
Cross references:
HPO:0002673 "Coxa valga" [Orphanet:46600]
Orphanet:46600 "Hip dislocation/dysplasia/coxa valga/coxa vara/coxa plana" [Orphanet:46600]
OMIM: "Bilateral coxa valga" [OMIM:Bilateral coxa valga]
UMLS:C0239137 "Coxa valga" [Orphanet:46600]
Is a (Direct Parents):
Orphanet Hip dysplasia
Orphanet Joint dislocation
HPO         Coxa valga
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:
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)