Abnormality of the foot

Symptom Information:

Symptom ID: HPO:0001760
Synonyms:
Abnormal feet morphology [HPO:0001760]
Abnormality of the feet [HPO:0001760]
Foot deformities [HPO:0001760]
Foot deformity [HPO:0001760]
Foot anomaly [Orphanet:22000]
Congenital deformity of foot (disorder) [Orphanet:22000]
Congenital Foot Deformity [Orphanet:22000]
Foot deformities [OMIM:Foot deformities]
Foot deformity [OMIM:Foot deformity]
Foot anomalies [Orphanet:22000]
Congenital foot malformation [Orphanet:22000]
Congenital foot malformation [MedDRA:10062332]
Anomalies of foot, congenital, not elsewhere classified [MedDRA:10062332]
Congenital foot malformation NOS [MedDRA:10062332]
Malformation foot [MedDRA:10062332]
Malformation foot NOS [MedDRA:10062332]
Other congenital anomalies of toes [MedDRA:10062332]
Other congenital deformities of feet [MedDRA:10062332]
Other congenital deformity of feet [MedDRA:10062332]
Metatarsal agenesis [MedDRA:10062332]
Foot agenesis [MedDRA:10062332]
Tarsal coalition [MedDRA:10062332]
Foot deformities (in some patients) [OMIM:Foot deformities (in some patients)]
Foot deformities (variable) [OMIM:Foot deformities (variable)]
Quality:
Cross references:
Orphanet:22000 "Foot anomalies" [Orphanet:22000]
OMIM: "Foot deformities" [OMIM:Foot deformities]
OMIM: "Foot deformity" [OMIM:Foot deformity]
OMIM: "Foot deformities (in some patients)" [OMIM:Foot deformities (in some patients)]
OMIM: "Foot deformities (variable)" [OMIM:Foot deformities (variable)]
UMLS:C0016508 "Congenital Foot Deformity" [Orphanet:22000]
Is a (Direct Parents):
HPO         Abnormality of the lower limb
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
Orphanet Abnormality of the lower limb
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)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396)
       Musculoskeletal and connective tissue disorders of limbs congenital(MedDRA:10028381)
          Abnormality of the foot(HPO:0001760)
Database Frequency: 96 / 7739
Resource:

All diseases associated with this symptom:

Achondrogenesis type 2 (Orphanet:93296)
Adult hypophosphatasia (Orphanet:247676)
Alpha-mannosidosis (Orphanet:61)
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 2N (Orphanet:228174)
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures (Orphanet:363454)
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures (Orphanet:209341)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type C (Orphanet:100045)
Autosomal dominant spastic paraplegia type 12 (Orphanet:100993)
Autosomal dominant spastic paraplegia type 9 (Orphanet:100990)
Autosomal recessive axonal neuropathy with neuromyotonia (Orphanet:324442)
Autosomal recessive distal osteolysis syndrome (Orphanet:2776)
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C (Orphanet:369867)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Bilateral renal agenesis (Orphanet:1848)
Blepharophimosis - ptosis - esotropia - syndactyly - short stature (Orphanet:2057)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
Brachydactyly type B (Orphanet:93383)
Branchiogenic deafness syndrome (Orphanet:50815)
COLD-INDUCED SWEATING SYNDROME 2 (OMIM:610313)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Central core disease (Orphanet:597)
Charcot-Marie-Tooth disease type 1A (Orphanet:101081)
Charcot-Marie-Tooth disease type 1B (Orphanet:101082)
Charcot-Marie-Tooth disease type 1E (Orphanet:90658)
Charcot-Marie-Tooth disease type 2B1 (Orphanet:98856)
Charcot-Marie-Tooth disease type 4B1 (Orphanet:99955)
Charcot-Marie-Tooth disease type 4B2 (Orphanet:99956)
Charcot-Marie-Tooth disease type 4C (Orphanet:99949)
Charcot-Marie-Tooth disease type 4D (Orphanet:99950)
Charcot-Marie-Tooth disease type 4G (Orphanet:99953)
Choreoacanthocytosis (Orphanet:2388)
Christianson syndrome (Orphanet:85278)
Cockayne syndrome (Orphanet:191)
Combined oxidative phosphorylation defect type 11 (Orphanet:324535)
Dejerine-Sottas syndrome (Orphanet:64748)
Dermatoosteolysis, Kirghizian type (Orphanet:1657)
Dystrophic epidermolysis bullosa (Orphanet:303)
Ectodermal dysplasia syndrome (Orphanet:79373)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Emery-Nelson syndrome (Orphanet:1927)
Fanconi anemia (Orphanet:84)
Fountain syndrome (Orphanet:3219)
Free sialic acid storage disease (Orphanet:834)
Free sialic acid storage disease, infantile form (Orphanet:309324)
Giant axonal neuropathy (Orphanet:643)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Growth delay - hydrocephaly - lung hypoplasia (Orphanet:3035)
Heart-hand syndrome type 3 (Orphanet:1342)
Hennekam syndrome (Orphanet:2136)
Hereditary sensory and autonomic neuropathy with spastic paraplegia (Orphanet:139578)
Joubert syndrome (Orphanet:475)
Joubert syndrome 2 (OMIM:608091)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 (OMIM:614563)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40 (OMIM:615599)
MYOPATHY, DISTAL, 3 (OMIM:610099)
Mesomelia-synostoses syndrome (Orphanet:2496)
Mesomelic dysplasia, Savarirayan type (Orphanet:85170)
Moderate multiminicore disease with hand involvement (Orphanet:178145)
Multiple osteochondromas (Orphanet:321)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC (OMIM:613640)
Nasu-Hakola disease (Orphanet:2770)
Navajo neurohepatopathy (Orphanet:255229)
Nevus comedonicus syndrome (Orphanet:64754)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Oculoosteocutaneous syndrome (Orphanet:2713)
PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS (OMIM:614369)
PONTOCEREBELLAR HYPOPLASIA, TYPE 1A (OMIM:607596)
PONTOCEREBELLAR HYPOPLASIA, TYPE 1B (OMIM:614678)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Pontocerebellar hypoplasia type 1 (Orphanet:2254)
Postaxial acrofacial dysostosis (Orphanet:246)
Progressive demyelinating neuropathy with bilateral striatal necrosis (Orphanet:217396)
Progressive pseudorheumatoid arthropathy of childhood (Orphanet:1159)
Refsum disease (Orphanet:773)
Roussy-Lévy syndrome (Orphanet:3115)
SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT (OMIM:616282)
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1 (OMIM:604320)
Scheie syndrome (Orphanet:93474)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Silver-Russell syndrome (Orphanet:813)
Spinocerebellar ataxia - dysmorphism (Orphanet:1185)
Spondylometaphyseal dysplasia, Kozlowski type (Orphanet:93314)
Steinert myotonic dystrophy (Orphanet:273)
Townes-Brocks syndrome (Orphanet:857)
Tricho-odonto-onychodysplasia - dominant syndactyly (Orphanet:3357)
Trisomy 20p (Orphanet:261318)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
Wolf-Hirschhorn syndrome (Orphanet:280)