Coxa vara

Symptom Information:

Symptom ID: HPO:0002812
Synonyms:
Hip joint varus deformity - observation [Orphanet:46600]
Coxa vara [OMIM:Coxa vara]
Hip dislocation/dysplasia/coxa valga/coxa vara/coxa plana [Orphanet:46600]
Coxa vara (rare) [OMIM:Coxa vara (rare)]
Quality:
Cross references:
Orphanet:46600 "Hip dislocation/dysplasia/coxa valga/coxa vara/coxa plana" [Orphanet:46600]
OMIM: "Coxa vara" [OMIM:Coxa vara]
OMIM: "Coxa vara (rare)" [OMIM:Coxa vara (rare)]
UMLS:C0239138 "Hip joint varus deformity - observation" [Orphanet:46600]
Is a (Direct Parents):
Orphanet Hip dysplasia
HPO         Abnormality of the femoral neck
Orphanet Joint dislocation
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 vara(HPO:0002812)
MedDRA:
Database Frequency: 58 / 7739
Resource:

All diseases associated with this symptom:

48,XXYY syndrome (Orphanet:10)
Acrocapitofemoral dysplasia (Orphanet:63446)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Axial spondylometaphyseal dysplasia (Orphanet:168549)
BRUCK SYNDROME 1 (OMIM:259450)
Bruck syndrome (Orphanet:2771)
CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME (OMIM:208250)
CARPENTER SYNDROME 2 (OMIM:614976)
CLEIDOCRANIAL DYSPLASIA (OMIM:119600)
COXA VARA (OMIM:122750)
Cleidocranial dysplasia (Orphanet:1452)
Czech dysplasia, metatarsal type (Orphanet:137678)
DESBUQUOIS DYSPLASIA 1 (OMIM:251450)
DWARFISM WITH TALL VERTEBRAE (OMIM:126950)
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED (OMIM:304950)
Desbuquois syndrome (Orphanet:1425)
EXOSTOSES, MULTIPLE, TYPE I (OMIM:133700)
EXOSTOSES, MULTIPLE, TYPE II (OMIM:133701)
Hurler syndrome (Orphanet:93473)
Kniest dysplasia (Orphanet:485)
MEIER-GORLIN SYNDROME 3 (OMIM:613803)
Metaphyseal anadysplasia (Orphanet:1040)
Metaphyseal chondrodysplasia, Schmid type (Orphanet:174)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Multiple epiphyseal dysplasia type 5 (Orphanet:93311)
Multiple epiphyseal dysplasia, Lowry type (Orphanet:166016)
Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia (Orphanet:166029)
Multiple osteochondromas (Orphanet:321)
OSTEOGENESIS IMPERFECTA, TYPE VI (OMIM:613982)
OSTEOGENESIS IMPERFECTA, TYPE VII (OMIM:610682)
OSTEOGENESIS IMPERFECTA, TYPE XI (OMIM:610968)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1 (OMIM:259700)
PATELLA APLASIA, COXA VARA, AND TARSAL SYNOSTOSIS (OMIM:168850)
Primordial short stature - microdontia - opalescent and rootless teeth (Orphanet:46658)
Progressive pseudorheumatoid arthropathy of childhood (Orphanet:1159)
Rhizomelic dysplasia, Patterson-Lowry type (Orphanet:2831)
SPINAL DYSPLASIA, ANHALT TYPE (OMIM:601344)
SPONASTRIME dysplasia (Orphanet:93357)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED (OMIM:313400)
SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE (OMIM:611702)
Schwartz-Jampel syndrome (Orphanet:800)
Shwachman-Diamond syndrome (Orphanet:811)
Spondylo-megaepiphyseal-metaphyseal dysplasia (Orphanet:228387)
Spondyloepimetaphyseal dysplasia - hypotrichosis (Orphanet:168443)
Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Orphanet:93346)
Spondyloepimetaphyseal dysplasia, Bieganski type (Orphanet:168448)
Spondyloepimetaphyseal dysplasia, Irapa type (Orphanet:93351)
Spondyloepimetaphyseal dysplasia, Missouri type (Orphanet:93356)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)
Spondyloepiphyseal dysplasia congenita (Orphanet:94068)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
Spondylometaphyseal dysplasia, 'corner fracture' type (Orphanet:93315)
Spondylometaphyseal dysplasia, Kozlowski type (Orphanet:93314)
Spondylometaphyseal dysplasia, Schmidt type (Orphanet:93316)
Steinert myotonic dystrophy (Orphanet:273)
Wolcott-Rallison syndrome (Orphanet:1667)
Wrinkly skin syndrome (Orphanet:2834)