Hallux valgus
Symptom Information:
Symptom ID: | HPO:0001822 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of digit(HPO:0011297) Abnormality of toe(HPO:0001780) Deviation of toes(HPO:0100498) Deviation of the hallux(HPO:0010051) Hallux valgus(HPO:0001822) Abnormality of the hallux(HPO:0001844) Deviation of the hallux(HPO:0010051) Hallux valgus(HPO:0001822) Abnormality of the lower limb(HPO:0002814) Abnormality of the foot(HPO:0001760) Abnormality of toe(HPO:0001780) Deviation of toes(HPO:0100498) Deviation of the hallux(HPO:0010051) Hallux valgus(HPO:0001822) Abnormality of the hallux(HPO:0001844) 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) |
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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) |