Coxa valga

Symptom Information:

Symptom ID: HPO:0002673
Synonyms:
COXA VALGA DEFORMITY [HPO:0002673]
Hip joint valgus deformity (finding) [Orphanet:46600]
Coxa valga [Orphanet:46600]
Coxa valga [OMIM:Coxa valga]
Coxa valga deformity [OMIM:Coxa valga deformity]
Hip dislocation/dysplasia/coxa valga/coxa vara/coxa plana [Orphanet:46600]
Quality:
Cross references:
HPO:0010665 "Bilateral coxa valga" [Orphanet:46600]
Orphanet:46600 "Hip dislocation/dysplasia/coxa valga/coxa vara/coxa plana" [Orphanet:46600]
OMIM: "Coxa valga" [OMIM:Coxa valga]
OMIM: "Coxa valga deformity" [OMIM:Coxa valga deformity]
UMLS:C0239137 "Coxa valga" [Orphanet:46600]
Is a (Direct Parents):
HPO         Abnormality of the femoral neck
Orphanet Hip dysplasia
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 valga(HPO:0002673)
MedDRA:
Database Frequency: 57 / 7739
Resource:

All diseases associated with this symptom:

48,XXYY syndrome (Orphanet:10)
AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVEFACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES (OMIM:109120)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
CARPENTER SYNDROME 1 (OMIM:201000)
CEREBROOCULOFACIOSKELETAL SYNDROME 1 (OMIM:214150)
COFFIN-SIRIS SYNDROME (OMIM:135900)
COFS syndrome (Orphanet:1466)
CRANIOMETADIAPHYSEAL DYSPLASIA (OMIM:269300)
Carpenter syndrome (Orphanet:65759)
Coffin-Lowry syndrome (Orphanet:192)
Coffin-Siris syndrome (Orphanet:1465)
Craniometadiaphyseal dysplasia, wormian bone type (Orphanet:85184)
DESBUQUOIS DYSPLASIA 1 (OMIM:251450)
DESBUQUOIS DYSPLASIA 2 (OMIM:615777)
Desbuquois syndrome (Orphanet:1425)
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 (OMIM:130070)
Ehlers-Danlos syndrome, progeroid type (Orphanet:75496)
Familial clubfoot due to 17q23.1q23.2 microduplication (Orphanet:238578)
Frontometaphyseal dysplasia (Orphanet:1826)
Fucosidosis (Orphanet:349)
GELEOPHYSIC DYSPLASIA 1 (OMIM:231050)
GM1 gangliosidosis type 2 (Orphanet:79256)
Geleophysic dysplasia (Orphanet:2623)
Hirsutism - skeletal dysplasia - intellectual deficit (Orphanet:2156)
Holoprosencephaly - craniosynostosis (Orphanet:2163)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Hypophosphatemic rickets, autosomal recessive, 2 (OMIM:613312)
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy (Orphanet:2958)
KAGAMI-OGATA SYNDROME (OMIM:608149)
Léri-Weill dyschondrosteosis (Orphanet:240)
MGAT2-CDG (Orphanet:79329)
Macular coloboma - cleft palate - hallux valgus (Orphanet:91494)
Marinesco-Sjögren syndrome (Orphanet:559)
Marshall syndrome (Orphanet:560)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 4A (Orphanet:309297)
Mucopolysaccharidosis type 4B (Orphanet:309310)
Multiple epiphyseal dysplasia, Beighton type (Orphanet:166011)
Occipital horn syndrome (Orphanet:198)
Ophthalmomandibulomelic dysplasia (Orphanet:2741)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Otopalatodigital syndrome type 1 (Orphanet:90650)
Schwartz-Jampel syndrome (Orphanet:800)
Singleton-Merten dysplasia (Orphanet:85191)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Spondyloepiphyseal dysplasia tarda, Kohn type (Orphanet:163665)
Spondylometaphyseal dysplasia, A4 type (Orphanet:168555)
Steinert myotonic dystrophy (Orphanet:273)
Thrombocytopenia - absent radius (Orphanet:3320)
Ulna metaphyseal dysplasia syndrome (Orphanet:1837)
Weaver syndrome (Orphanet:3447)
Wolcott-Rallison syndrome (Orphanet:1667)
X-linked spondyloepimetaphyseal dysplasia (Orphanet:93349)