Genu valgum

Symptom Information:

Symptom ID: HPO:0002857
Synonyms:
Genu valga [HPO:0002857]
genu valgum or genu varum [HPO:0002857]
Genu valgus [HPO:0002857]
Genua valga [HPO:0002857]
Knee joint valgus deformity [HPO:0002857]
Knock knees [HPO:0002857]
Knee joint valgus deformity (finding) [Orphanet:21440]
Knee joint valgus deformity [Orphanet:21440]
Genu valga [OMIM:Genu valga]
Genu valgum [OMIM:Genu valgum]
Genu valgum or genu varum [OMIM:Genu valgum or genu varum]
Genu valgus [OMIM:Genu valgus]
Genua valga [OMIM:Genua valga]
Genu valgum [Orphanet:21440]
Knock-knee [HPO:0002857]
Knock-knee [Orphanet:21440]
Knee deformity [MedDRA:10062061]
Genu recurvatum (acquired) [MedDRA:10062061]
Genu valgum [MedDRA:10062061]
Genu valgum (acquired) [MedDRA:10062061]
Genu valgum or varum (acquired) [MedDRA:10062061]
Genu varum [MedDRA:10062061]
Genu varum (acquired) [MedDRA:10062061]
Knee deformity (acquired) [MedDRA:10062061]
Knee deformity NOS [MedDRA:10062061]
Knock-knee [MedDRA:10062061]
Other acquired deformities of knee [MedDRA:10062061]
Bow legs [MedDRA:10062061]
Genu recurvatum (1 family) [OMIM:Genu recurvatum (1 family)]
Genu recurvatum (in some patients) [OMIM:Genu recurvatum (in some patients)]
Genu valga (80% of patients) [OMIM:Genu valga (80% of patients)]
Genu valgum (present at 1 year) [OMIM:Genu valgum (present at 1 year)]
Genu valgum (rare) [OMIM:Genu valgum (rare)]
Genu varum or valgum [OMIM:Genu varum or valgum]
Leg bowing [OMIM:Leg bowing]
Quality:
Cross references:
Orphanet:21440 "Genu valgum" [Orphanet:21440]
OMIM: "Genu valga" [OMIM:Genu valga]
OMIM: "Genu valgum" [OMIM:Genu valgum]
OMIM: "Genu valgum or genu varum" [OMIM:Genu valgum or genu varum]
OMIM: "Genu valgus" [OMIM:Genu valgus]
OMIM: "Genua valga" [OMIM:Genua valga]
OMIM: "Genu recurvatum (1 family)" [OMIM:Genu recurvatum (1 family)]
OMIM: "Genu recurvatum (in some patients)" [OMIM:Genu recurvatum (in some patients)]
OMIM: "Genu valga (80% of patients)" [OMIM:Genu valga (80% of patients)]
OMIM: "Genu valgum (present at 1 year)" [OMIM:Genu valgum (present at 1 year)]
OMIM: "Genu valgum (rare)" [OMIM:Genu valgum (rare)]
OMIM: "Genu varum or valgum" [OMIM:Genu varum or valgum]
OMIM: "Leg bowing" [OMIM:Leg bowing]
UMLS:C0576093 "Knee joint valgus deformity" [Orphanet:21440]
Is a (Direct Parents):
HPO         Abnormality of the knee
Orphanet Abnormality of the knee
HPO         Bowing of the legs
MedDRA Extremity deformities
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 joint morphology(HPO:0001367)
                Abnormality of lower limb joint(HPO:0100491)
                   Abnormality of the knee(HPO:0002815)
                      Genu valgum(HPO:0002857)
             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 valgum(HPO:0002857)
             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 valgum(HPO:0002857)
                      Abnormality of lower limb joint(HPO:0100491)
                         Abnormality of the knee(HPO:0002815)
                            Genu valgum(HPO:0002857)
                   Anomaly of the limb diaphyses(HPO:0006504)
                      Bowing of the long bones(HPO:0006487)
                         Bowing of the legs(HPO:0002979)
                            Genu valgum(HPO:0002857)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue deformities (incl intervertebral disc disorders)(MedDRA:10028377)
       Extremity deformities(MedDRA:10012139)
          Genu valgum(HPO:0002857)
Database Frequency: 144 / 7739
Resource:

All diseases associated with this symptom:

Acro-oto-ocular syndrome (Orphanet:2980)
Acrocraniofacial dysostosis (Orphanet:949)
Albers-Schönberg osteopetrosis (Orphanet:53)
Alpha-mannosidosis (Orphanet:61)
Aromatase deficiency (Orphanet:91)
Atkin-Flaitz syndrome (Orphanet:1193)
Autosomal recessive Stickler syndrome (Orphanet:250984)
Beta-thalassemia major (Orphanet:231214)
Brachytelephalangy - dysmorphism - Kallmann syndrome (Orphanet:1295)
CARPENTER SYNDROME 1 (OMIM:201000)
CHST3-related skeletal dysplasia (Orphanet:263463)
CLARK-BARAITSER SYNDROME (OMIM:300602)
CODAS syndrome (Orphanet:1458)
CRANIOMETADIAPHYSEAL DYSPLASIA (OMIM:269300)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Camurati-Engelmann disease (Orphanet:1328)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carpenter syndrome (Orphanet:65759)
Carpenter-Waziri syndrome (Orphanet:93973)
Cataract - intellectual deficit - anal atresia - urinary defects (Orphanet:1381)
Childhood-onset hypophosphatasia (Orphanet:247667)
Chondrodysplasia with joint dislocations, gPAPP type (Orphanet:280586)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Classical homocystinuria (Orphanet:394)
Cleidocranial dysplasia (Orphanet:1452)
Coats plus syndrome (Orphanet:313838)
Cohen syndrome (Orphanet:193)
Cystinosis (Orphanet:213)
DYGGVE-MELCHIOR-CLAUSEN DISEASE (OMIM:223800)
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED (OMIM:304950)
Dent disease type 1 (Orphanet:93622)
Disorder of sex development - intellectual deficit (Orphanet:2983)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Dysmorphism - pectus carinatum - joint laxity (Orphanet:2104)
Dysplasia epiphysealis hemimelica (Orphanet:1822)
Dysspondyloenchondromatosis (Orphanet:85198)
EPIPHYSEAL DYSPLASIA, BAUMANN TYPE (OMIM:610797)
EXOSTOSES, MULTIPLE, TYPE I (OMIM:133700)
EXOSTOSES, MULTIPLE, TYPE II (OMIM:133701)
Ear-patella-short stature syndrome (Orphanet:2554)
Ellis Van Creveld syndrome (Orphanet:289)
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria (Orphanet:1035)
Facial dysmorphism - shawl scrotum - joint laxity (Orphanet:1778)
Familial clubfoot due to 17q23.1q23.2 microduplication (Orphanet:238578)
Frontometaphyseal dysplasia (Orphanet:1826)
GENU VALGUM, ST. HELENA FAMILIAL (OMIM:137370)
Gnathodiaphyseal dysplasia (Orphanet:53697)
HAJDU-CHENEY SYNDROME (OMIM:102500)
Holmes-Gang syndrome (Orphanet:93970)
Humerus trochlea aplasia (Orphanet:3383)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Hypophosphatemic rickets, autosomal recessive, 2 (OMIM:613312)
Intellectual deficit - cataracts - calcified pinnae - myopathy (Orphanet:3042)
Intellectual deficit, X-linked, Stevenson type (Orphanet:85325)
Juberg-Marsidi syndrome (Orphanet:93972)
Langer-Giedion syndrome (Orphanet:502)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Leri pleonosteosis (Orphanet:2900)
Lipodystrophy - intellectual deficit - deafness (Orphanet:50811)
Léri-Weill dyschondrosteosis (Orphanet:240)
MEIER-GORLIN SYNDROME 1 (OMIM:224690)
MUCOLIPIDOSIS III GAMMA (OMIM:252605)
Macular coloboma - cleft palate - hallux valgus (Orphanet:91494)
Marden-Walker syndrome (Orphanet:2461)
Marshall syndrome (Orphanet:560)
Megalencephaly (Orphanet:2477)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Mesomelia-synostoses syndrome (Orphanet:2496)
Mesomelic dwarfism, Nievergelt type (Orphanet:2633)
Metaphyseal chondrodysplasia, Spahr type (Orphanet:2501)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Mikati-Najjar-Sahli syndrome (Orphanet:2558)
Mucopolysaccharidosis type 3 (Orphanet:581)
Mucopolysaccharidosis type 4 (Orphanet:582)
Mucopolysaccharidosis type 4A (Orphanet:309297)
Mucopolysaccharidosis type 4B (Orphanet:309310)
Mucopolysaccharidosis type 6 (Orphanet:583)
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, Al-Gazali type (Orphanet:166024)
Multiple epiphyseal dysplasia, Beighton type (Orphanet:166011)
Multiple epiphyseal dysplasia, Lowry type (Orphanet:166016)
Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia (Orphanet:166029)
Multiple non-ossifying fibromatosis (Orphanet:2029)
Multiple osteochondromas (Orphanet:321)
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion (Orphanet:363700)
Non-eruption of teeth - maxillary hypoplasia - genu valgum (Orphanet:2972)
OSTEOGENESIS IMPERFECTA, TYPE X (OMIM:613848)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2 (OMIM:259710)
OTOFACIOOSSEOUS-GONADAL SYNDROME (OMIM:601976)
Occipital horn syndrome (Orphanet:198)
Oculocerebrorenal syndrome (Orphanet:534)
Oculofaciocardiodental syndrome (Orphanet:2712)
Osteochondrodysplatic nanism - deafness - retinitis pigmentosa (Orphanet:2653)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Osteogenesis imperfecta (Orphanet:666)
Osteopetrosis (Orphanet:2781)
Osteopetrosis with renal tubular acidosis (Orphanet:2785)
Parastremmatic dwarfism (Orphanet:2646)
Prolidase deficiency (Orphanet:742)
Pseudoachondroplasia (Orphanet:750)
Pseudoleprechaunism syndrome, Patterson type (Orphanet:2976)
Pyle disease (Orphanet:3005)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Rhizomelic dysplasia, Patterson-Lowry type (Orphanet:2831)
Richieri Costa-da Silva syndrome (Orphanet:3101)
SANTOS SYNDROME (OMIM:613005)
SATOYOSHI SYNDROME (OMIM:600705)
SMITH-MCCORT DYSPLASIA 1 (OMIM:607326)
SMITH-MCCORT DYSPLASIA 2 (OMIM:615222)
SOTOS SYNDROME 1 (OMIM:117550)
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE (OMIM:614066)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE (OMIM:609223)
Scheie syndrome (Orphanet:93474)
Schnyder corneal dystrophy (Orphanet:98967)
Schwartz-Jampel syndrome (Orphanet:800)
Short-rib thoracic dysplasia 10 with or without polydactyly (OMIM:615630)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Singleton-Merten dysplasia (Orphanet:85191)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Smith-McCort dysplasia (Orphanet:178355)
Sotos syndrome (Orphanet:821)
Spondylo-megaepiphyseal-metaphyseal dysplasia (Orphanet:228387)
Spondyloepimetaphyseal dysplasia - abnormal dentition (Orphanet:168451)
Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Orphanet:93346)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Spondyloepimetaphyseal dysplasia with multiple dislocations (Orphanet:93360)
Spondyloepimetaphyseal dysplasia, Irapa type (Orphanet:93351)
Spondyloepiphyseal dysplasia, Kimberley type (Orphanet:93283)
Spondyloepiphyseal dysplasia, Maroteaux type (Orphanet:263482)
Spondylometaphyseal dysplasia, 'corner fracture' type (Orphanet:93315)
Spondylometaphyseal dysplasia, Kozlowski type (Orphanet:93314)
Spondylometaphyseal dysplasia, Schmidt type (Orphanet:93316)
Stickler syndrome (Orphanet:828)
Stüve-Wiedemann syndrome (Orphanet:3206)
Summitt syndrome (Orphanet:3210)
Thoracomelic dysplasia (Orphanet:1803)
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR (OMIM:600785)
Williams syndrome (Orphanet:904)
Wolcott-Rallison syndrome (Orphanet:1667)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)