Hallux valgus

Symptom Information:

Symptom ID: HPO:0001822
Synonyms:
Lateral deviation of great toe [HPO:0001822]
Lateral deviation of halluces [HPO:0001822]
Congenital hallux valgus (disorder) [Orphanet:22600]
Hallux valgus (disorder) [Orphanet:22600]
Hallux Valgus [Orphanet:22600]
Congenital hallux valgus [Orphanet:22600]
Hallux valgus [OMIM:Hallux valgus]
Lateral deviation of great toe [OMIM:Lateral deviation of great toe]
Lateral deviation of halluces [OMIM:Lateral deviation of halluces]
Hallux valgus [Orphanet:22600]
Foot deformity [MedDRA:10061159]
Acquired deformities of toe [MedDRA:10061159]
Acquired equinovarus deformity [MedDRA:10061159]
Cavovarus deformity of foot, acquired [MedDRA:10061159]
Cavus deformity of foot, acquired [MedDRA:10061159]
Claw foot, acquired [MedDRA:10061159]
Equinus deformity of foot, acquired [MedDRA:10061159]
Fallen arches [MedDRA:10061159]
Flat feet [MedDRA:10061159]
Flat foot [MedDRA:10061159]
Foot deformity NOS [MedDRA:10061159]
Hallux malleus [MedDRA:10061159]
Hallux rigidus [MedDRA:10061159]
Hallux valgus [MedDRA:10061159]
Hallux valgus (acquired) [MedDRA:10061159]
Hallux varus (acquired) [MedDRA:10061159]
Hammer toe [MedDRA:10061159]
Other acquired calcaneus deformity [MedDRA:10061159]
Other acquired deformities of toe [MedDRA:10061159]
Other hammer toe (acquired) [MedDRA:10061159]
Pes cavus [MedDRA:10061159]
Pes planus [MedDRA:10061159]
Pes valgus [MedDRA:10061159]
Toe deformities (acquired) [MedDRA:10061159]
Toe deformities NOS [MedDRA:10061159]
Unspecified acquired deformity of toe [MedDRA:10061159]
Toe deformity [MedDRA:10061159]
Pigeon toe [MedDRA:10061159]
In-toeing [MedDRA:10061159]
Out-toeing [MedDRA:10061159]
Metatarsus primus elevatus [MedDRA:10061159]
Splayfoot [MedDRA:10061159]
Talipes valgus acquired [MedDRA:10061159]
Bunionette [MedDRA:10061159]
Flat feet (female) [OMIM:Flat feet (female)]
Foot deformities (in some patients) [OMIM:Foot deformities (in some patients)]
Foot deformities (variable) [OMIM:Foot deformities (variable)]
Hallux valgus (in some patients) [OMIM:Hallux valgus (in some patients)]
Hammer toe (2-4 toes) [OMIM:Hammer toe (2-4 toes)]
Hammer toes [OMIM:Hammer toes]
Pes cavus (1 family) [OMIM:Pes cavus (1 family)]
Pes cavus (1 patient) [OMIM:Pes cavus (1 patient)]
Pes cavus (17%) [OMIM:Pes cavus (17%)]
Pes cavus (in 1 family) [OMIM:Pes cavus (in 1 family)]
Pes cavus (in some patients) [OMIM:Pes cavus (in some patients)]
Pes cavus (less common) [OMIM:Pes cavus (less common)]
Pes cavus (uncommon) [OMIM:Pes cavus (uncommon)]
Pes planus (1 family) [OMIM:Pes planus (1 family)]
Pes planus (rare) [OMIM:Pes planus (rare)]
Pes valgus [OMIM:Pes valgus]
Quality:
Cross references:
Orphanet:22600 "Hallux valgus" [Orphanet:22600]
OMIM: "Hallux valgus" [OMIM:Hallux valgus]
OMIM: "Lateral deviation of great toe" [OMIM:Lateral deviation of great toe]
OMIM: "Lateral deviation of halluces" [OMIM:Lateral deviation of halluces]
OMIM: "Flat feet (female)" [OMIM:Flat feet (female)]
OMIM: "Foot deformities (in some patients)" [OMIM:Foot deformities (in some patients)]
OMIM: "Foot deformities (variable)" [OMIM:Foot deformities (variable)]
OMIM: "Hallux valgus (in some patients)" [OMIM:Hallux valgus (in some patients)]
OMIM: "Hammer toe (2-4 toes)" [OMIM:Hammer toe (2-4 toes)]
OMIM: "Hammer toes" [OMIM:Hammer toes]
OMIM: "Pes cavus (1 family)" [OMIM:Pes cavus (1 family)]
OMIM: "Pes cavus (1 patient)" [OMIM:Pes cavus (1 patient)]
OMIM: "Pes cavus (17%)" [OMIM:Pes cavus (17%)]
OMIM: "Pes cavus (in 1 family)" [OMIM:Pes cavus (in 1 family)]
OMIM: "Pes cavus (in some patients)" [OMIM:Pes cavus (in some patients)]
OMIM: "Pes cavus (less common)" [OMIM:Pes cavus (less common)]
OMIM: "Pes cavus (uncommon)" [OMIM:Pes cavus (uncommon)]
OMIM: "Pes planus (1 family)" [OMIM:Pes planus (1 family)]
OMIM: "Pes planus (rare)" [OMIM:Pes planus (rare)]
OMIM: "Pes valgus" [OMIM:Pes valgus]
UMLS:C0018536 "Hallux Valgus" [Orphanet:22600]
UMLS:C0265656 "Congenital hallux valgus" [Orphanet:22600]
Is a (Direct Parents):
Orphanet Abnormality of the hallux
HPO         Deviation of the hallux
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 appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of the foot(HPO:0001760)
                         Abnormality of toe(HPO:0001780)
                            Abnormality of the hallux(HPO:0001844)
                               Deviation of the hallux(HPO:0010051)
                                  Hallux valgus(HPO:0001822)
                            Deviation of toes(HPO:0100498)
                               Deviation of the hallux(HPO:0010051)
                                  Hallux valgus(HPO:0001822)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of toe(HPO:0001780)
                         Abnormality of the hallux(HPO:0001844)
                            Deviation of the hallux(HPO:0010051)
                               Hallux valgus(HPO:0001822)
                         Deviation of toes(HPO:0100498)
                            Deviation of the hallux(HPO:0010051)
                               Hallux valgus(HPO:0001822)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue deformities (incl intervertebral disc disorders)(MedDRA:10028377)
       Extremity deformities(MedDRA:10012139)
          Hallux valgus(HPO:0001822)
Database Frequency: 70 / 7739
Resource:

All diseases associated with this symptom:

17q11 microdeletion syndrome (Orphanet:97685)
17q11.2 microduplication syndrome (Orphanet:139474)
ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES (OMIM:208080)
Acro-cardio-facial syndrome (Orphanet:2008)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Autosomal dominant Charcot-Marie-Tooth disease type 2A1 (Orphanet:99946)
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (Orphanet:99947)
Autosomal dominant Charcot-Marie-Tooth disease type 2B (Orphanet:99936)
Autosomal dominant Charcot-Marie-Tooth disease type 2E (Orphanet:99939)
Autosomal dominant Charcot-Marie-Tooth disease type 2G (Orphanet:99941)
Autosomal dominant Charcot-Marie-Tooth disease type 2P (Orphanet:300319)
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures (Orphanet:209341)
Autosomal dominant spastic paraplegia type 31 (Orphanet:101011)
Autosomal recessive centronuclear myopathy (Orphanet:169186)
Autosomal recessive cerebelloparenchymal disorder type 3 (Orphanet:1170)
Autosomal recessive spastic paraplegia type 46 (Orphanet:320391)
Autosomal recessive spastic paraplegia type 5A (Orphanet:100986)
Brachydactyly type A2 (Orphanet:93396)
Brachydactyly-syndactyly, Zhao type (Orphanet:93409)
CRANIOSYNOSTOSIS, ADELAIDE TYPE (OMIM:600593)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Camptodactyly syndrome, Guadalajara type 2 (Orphanet:1326)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Charcot-Marie-Tooth disease type 1A (Orphanet:101081)
Charcot-Marie-Tooth disease type 1B (Orphanet:101082)
Cranioectodermal dysplasia 4 (OMIM:614378)
Craniosynostosis and dental anomalies (Orphanet:284149)
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED (OMIM:304950)
Dejerine-Sottas syndrome (Orphanet:64748)
Ehlers-Danlos syndrome type 1 (Orphanet:90309)
Faisalabad histiocytosis (Orphanet:254707)
Feingold syndrome (Orphanet:1305)
Fibrodysplasia ossificans progressiva (Orphanet:337)
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT (OMIM:610100)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
H syndrome (Orphanet:168569)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
Isolated plagiocephaly (Orphanet:35098)
Jawad syndrome (Orphanet:313795)
Leri pleonosteosis (Orphanet:2900)
Limb-mammary syndrome (Orphanet:69085)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 (OMIM:614563)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 7 (OMIM:614104)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 (OMIM:611091)
MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES (OMIM:606772)
Macular coloboma - cleft palate - hallux valgus (Orphanet:91494)
Marfan syndrome type 1 (Orphanet:284963)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Mowat-Wilson syndrome (Orphanet:2152)
Mucopolysaccharidosis type 2 (Orphanet:580)
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID (OMIM:615575)
NEUROPATHY, HEREDITARY SENSORY, TYPE IF (OMIM:615632)
Nager syndrome (Orphanet:245)
Oculofaciocardiodental syndrome (Orphanet:2712)
Pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome (Orphanet:254723)
Pitt-Hopkins syndrome (Orphanet:2896)
Proteus syndrome (Orphanet:744)
Rosaï-Dorfman disease (Orphanet:158014)
Roussy-Lévy syndrome (Orphanet:3115)
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE (OMIM:614066)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 (OMIM:606002)
Saethre-Chotzen syndrome (Orphanet:794)
Short-rib thoracic dysplasia 5 with or without polydactyly (OMIM:614376)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Trismus - pseudocamptodactyly (Orphanet:3377)
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME (OMIM:300280)
Van den Ende-Gupta syndrome (Orphanet:2460)
Williams syndrome (Orphanet:904)
X-linked creatine transporter deficiency (Orphanet:52503)
Young adult-onset distal hereditary motor neuropathy (Orphanet:314485)