Genu varum

Symptom Information:

Symptom ID: HPO:0002970
Synonyms:
Bow legs [HPO:0002970]
Bow-leggedness [HPO:0002970]
Genu vara [HPO:0002970]
Genua vara [HPO:0002970]
Knee joint - varus deformity [HPO:0002970]
Knee joint - varus deformity (finding) [Orphanet:21480]
Genu varum [Orphanet:21480]
Genu vara [OMIM:Genu vara]
Genu varum [OMIM:Genu varum]
Genua vara [OMIM:Genua vara]
Leg bowing [OMIM:Leg bowing]
Quality:
Cross references:
Orphanet:21480 "Genu varum" [Orphanet:21480]
OMIM: "Genu vara" [OMIM:Genu vara]
OMIM: "Genu varum" [OMIM:Genu varum]
OMIM: "Genua vara" [OMIM:Genua vara]
OMIM: "Leg bowing" [OMIM:Leg bowing]
UMLS:C0544755 "Genu varum" [Orphanet:21480]
Is a (Direct Parents):
Orphanet Abnormality of the knee
HPO         Bowing of the legs
HPO         Abnormality of the knee
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)
             Abnormality of long bone morphology(HPO:0011314)
                Abnormal diaphysis morphology(HPO:0000940)
                   Anomaly of the limb diaphyses(HPO:0006504)
                      Bowing of the long bones(HPO:0006487)
                         Bowing of the legs(HPO:0002979)
                            Genu varum(HPO:0002970)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the lower limb(HPO:0002814)
                      Bowing of the legs(HPO:0002979)
                         Genu varum(HPO:0002970)
                      Abnormality of lower limb joint(HPO:0100491)
                         Abnormality of the knee(HPO:0002815)
                            Genu varum(HPO:0002970)
                   Anomaly of the limb diaphyses(HPO:0006504)
                      Bowing of the long bones(HPO:0006487)
                         Bowing of the legs(HPO:0002979)
                            Genu varum(HPO:0002970)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of lower limb joint(HPO:0100491)
                   Abnormality of the knee(HPO:0002815)
                      Genu varum(HPO:0002970)
MedDRA:
Database Frequency: 60 / 7739
Resource:

All diseases associated with this symptom:

Achondroplasia (Orphanet:15)
Acrocapitofemoral dysplasia (Orphanet:63446)
Aortic arch anomaly - peculiar facies - intellectual deficit (Orphanet:1110)
BARATELA-SCOTT SYNDROME (OMIM:300881)
BLOUNT DISEASE, ADOLESCENT (OMIM:259200)
Blount disease (Orphanet:2768)
CRANIOMETADIAPHYSEAL DYSPLASIA (OMIM:269300)
Carpenter syndrome (Orphanet:65759)
DESBUQUOIS DYSPLASIA 1 (OMIM:251450)
Desbuquois syndrome (Orphanet:1425)
Dysplasia epiphysealis hemimelica (Orphanet:1822)
Ear-patella-short stature syndrome (Orphanet:2554)
FACES syndrome (Orphanet:1969)
Gnathodiaphyseal dysplasia (Orphanet:53697)
Goldblatt syndrome (Orphanet:166272)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Hypochondroplasia (Orphanet:429)
Hypophosphatemic rickets, autosomal recessive, 2 (OMIM:613312)
Ito hypomelanosis (Orphanet:435)
Léri-Weill dyschondrosteosis (Orphanet:240)
MEIER-GORLIN SYNDROME 3 (OMIM:613803)
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS (OMIM:250460)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Mesomelic dwarfism, Nievergelt type (Orphanet:2633)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Metaphyseal anadysplasia (Orphanet:1040)
Metaphyseal chondrodysplasia, Schmid type (Orphanet:174)
Metaphyseal chondrodysplasia, Spahr type (Orphanet:2501)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Microspherophakia - metaphyseal dysplasia (Orphanet:2551)
Multiple epiphyseal dysplasia due to collagen 9 anomaly (Orphanet:166002)
Multiple epiphyseal dysplasia type 1 (Orphanet:93308)
Multiple epiphyseal dysplasia type 5 (Orphanet:93311)
Multiple epiphyseal dysplasia, with miniepiphyses (Orphanet:166032)
Multiple non-ossifying fibromatosis (Orphanet:2029)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Pachydermoperiostosis (Orphanet:2796)
Pacman dysplasia (Orphanet:1952)
Parastremmatic dwarfism (Orphanet:2646)
Phocomelia - ectrodactyly - deafness - sinus arrhythmia (Orphanet:2878)
Platyspondylic dysplasia, Torrance type (Orphanet:85166)
Progressive pseudorheumatoid arthropathy of childhood (Orphanet:1159)
Pseudoachondroplasia (Orphanet:750)
SMITH-MCCORT DYSPLASIA 1 (OMIM:607326)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE (OMIM:609223)
SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE (OMIM:611702)
Satoyoshi syndrome (Orphanet:3130)
Smith-McCort dysplasia (Orphanet:178355)
Sotos syndrome (Orphanet:821)
Spondylo-megaepiphyseal-metaphyseal dysplasia (Orphanet:228387)
Spondyloepimetaphyseal dysplasia - hypotrichosis (Orphanet:168443)
Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Orphanet:93346)
Spondyloepimetaphyseal dysplasia with multiple dislocations (Orphanet:93360)
Spondyloepimetaphyseal dysplasia, Missouri type (Orphanet:93356)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)
Spondyloepiphyseal dysplasia, Kimberley type (Orphanet:93283)
Temtamy syndrome (Orphanet:1777)
Thrombocytopenia - absent radius (Orphanet:3320)
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR (OMIM:600785)
X-linked hypophosphatemia (Orphanet:89936)