Genu valgum
Symptom Information:
Symptom ID: | HPO:0002857 | |||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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 valgum(HPO:0002857) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Anomaly of the limb diaphyses(HPO:0006504) Bowing of the long bones(HPO:0006487) Bowing of the legs(HPO:0002979) Genu valgum(HPO:0002857) Abnormality of the lower limb(HPO:0002814) Abnormality of lower limb joint(HPO:0100491) Abnormality of the knee(HPO:0002815) Genu valgum(HPO:0002857) Bowing of the legs(HPO:0002979) Genu valgum(HPO:0002857) Abnormal joint morphology(HPO:0001367) Abnormality of lower limb joint(HPO:0100491) Abnormality of the knee(HPO:0002815) 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) |
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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) |