Abnormality of the foot
Symptom Information:
Symptom ID: | HPO:0001760 | ||||||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||||||
Quality: | |||||||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||||||||
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) |