Pes planus

Symptom Information:

Symptom ID: HPO:0001763
Synonyms:
Dropped arches [HPO:0001763]
Fallen arches [HPO:0001763]
Flat feet [HPO:0001763]
Congenital pes planus (disorder) [Orphanet:22120]
Pes planus (disorder) [Orphanet:22120]
Flatfoot [HPO:0001763]
Flatfoot [Orphanet:22120]
Flat feet [OMIM:Flat feet]
Pes planus [OMIM:Pes planus]
Flat foot [Orphanet:22120]
Pes valgus [Orphanet:22120]
Congenital flat feet [Orphanet:22120]
Pes planus [Orphanet:22120]
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]
Congenital flat feet [MedDRA:10010475]
Pes planus, congenital [MedDRA:10010475]
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:22120 "Flat foot" [Orphanet:22120]
OMIM: "Flat feet" [OMIM:Flat feet]
OMIM: "Pes planus" [OMIM:Pes planus]
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:C0016202 "Flatfoot" [HPO:0001763]
UMLS:C0016202 "Flatfoot" [Orphanet:22120]
Is a (Direct Parents):
Orphanet Abnormality of the foot
MedDRA Extremity deformities
HPO         Abnormality of the foot
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
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)
                         Pes planus(HPO:0001763)
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)
          Pes planus(HPO:0001763)
    Musculoskeletal and connective tissue deformities (incl intervertebral disc disorders)(MedDRA:10028377)
       Extremity deformities(MedDRA:10012139)
          Pes planus(HPO:0001763)
Database Frequency: 176 / 7739
Resource:

All diseases associated with this symptom:

16p13.11 microduplication syndrome (Orphanet:261243)
17q11 microdeletion syndrome (Orphanet:97685)
17q11.2 microduplication syndrome (Orphanet:139474)
17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
3M syndrome (Orphanet:2616)
3q29 microduplication (Orphanet:251038)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
49,XXXXY syndrome (Orphanet:96264)
AARSKOG SYNDROME, AUTOSOMAL DOMINANT (OMIM:100050)
AREDYLD syndrome (Orphanet:1133)
ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED (OMIM:300158)
ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES (OMIM:208080)
Aarskog-Scott syndrome (Orphanet:915)
Acro-renal-ocular syndrome (Orphanet:959)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Alström syndrome (Orphanet:64)
Aneurysm - osteoarthritis syndrome (Orphanet:284984)
Aspartylglucosaminuria (Orphanet:93)
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 congenital benign spinal muscular atrophy (Orphanet:1216)
Autosomal dominant spastic paraplegia type 31 (Orphanet:101011)
Autosomal recessive centronuclear myopathy (Orphanet:169186)
Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome (Orphanet:363429)
Autosomal recessive cerebelloparenchymal disorder type 3 (Orphanet:1170)
Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency (Orphanet:324262)
Autosomal recessive cutis laxa type 2A (Orphanet:357058)
Autosomal recessive spastic paraplegia type 46 (Orphanet:320391)
Autosomal recessive spastic paraplegia type 5A (Orphanet:100986)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME1 (OMIM:224050)
CHST3-related skeletal dysplasia (Orphanet:263463)
Cabezas syndrome (Orphanet:85293)
Camurati-Engelmann disease (Orphanet:1328)
Carpenter-Waziri syndrome (Orphanet:93973)
Central core disease (Orphanet:597)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Charcot-Marie-Tooth disease type 1A (Orphanet:101081)
Charcot-Marie-Tooth disease type 1B (Orphanet:101082)
Charcot-Marie-Tooth disease type 4B3 (Orphanet:363981)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Coffin-Lowry syndrome (Orphanet:192)
Cohen syndrome (Orphanet:193)
Cold-induced sweating syndrome (Orphanet:157820)
Coxo-podo-patellar syndrome (Orphanet:1509)
Cranioectodermal dysplasia 4 (OMIM:614378)
Craniolenticulosutural dysplasia (Orphanet:50814)
Craniosynostosis and dental anomalies (Orphanet:284149)
DESBUQUOIS DYSPLASIA 1 (OMIM:251450)
DESBUQUOIS DYSPLASIA 2 (OMIM:615777)
Dejerine-Sottas syndrome (Orphanet:64748)
Desbuquois syndrome (Orphanet:1425)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal hereditary motor neuropathy type 5 (Orphanet:139536)
Dubowitz syndrome (Orphanet:235)
Dysequilibrium syndrome (Orphanet:1766)
Dysplasia epiphysealis hemimelica (Orphanet:1822)
EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE (OMIM:608763)
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 (OMIM:130070)
EPIPHYSEAL DYSPLASIA, BAUMANN TYPE (OMIM:610797)
Ehlers-Danlos syndrome type 1 (Orphanet:90309)
Ehlers-Danlos syndrome type 2 (Orphanet:90318)
Ehlers-Danlos syndrome, cardiac valvular type (Orphanet:230851)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type (Orphanet:300179)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Ehlers-Danlos syndrome, progeroid type (Orphanet:75496)
Ehlers-Danlos syndrome, spondylocheirodysplastic type (Orphanet:157965)
Fanconi anemia (Orphanet:84)
Fragile X syndrome (Orphanet:908)
Friedreich ataxia 1 (OMIM:229300)
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT (OMIM:610100)
Geroderma osteodysplastica (Orphanet:2078)
Giant axonal neuropathy (Orphanet:643)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA (OMIM:244200)
Haim-Munk syndrome (Orphanet:2342)
Holmes-Gang syndrome (Orphanet:93970)
Hypertryptophanemia (Orphanet:2224)
Ichthyosis-cheek-eyebrow syndrome (Orphanet:2267)
Infantile-onset autosomal recessive nonprogressive cerebellar ataxia (Orphanet:284332)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
Intellectual deficit, X-linked, Nascimento type (Orphanet:163956)
Intellectual deficit, X-linked, Raymond type (Orphanet:163953)
Isolated plagiocephaly (Orphanet:35098)
Jacobsen syndrome (Orphanet:2308)
Juberg-Marsidi syndrome (Orphanet:93972)
LOEYS-DIETZ SYNDROME 4 (OMIM:614816)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Lipodystrophy due to peptidic growth factors deficiency (Orphanet:1979)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
Lower motor neuron syndrome with late-adult onset (Orphanet:276435)
MACS syndrome (Orphanet:217335)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 (OMIM:614563)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 17 (OMIM:615009)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44 (OMIM:615942)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 (OMIM:611091)
MENTAL RETARDATION, X-LINKED 93 (OMIM:300659)
MGAT2-CDG (Orphanet:79329)
MICROPHTHALMIA, SYNDROMIC 14 (OMIM:615877)
MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY (OMIM:259600)
MYASTHENIC SYNDROME, CONGENITAL, 14 (OMIM:616228)
Marfan syndrome (Orphanet:558)
Marfan syndrome type 1 (Orphanet:284963)
Marinesco-Sjögren syndrome (Orphanet:559)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Microduplication Xp11.22-p11.23 syndrome (Orphanet:217377)
Mietens syndrome (Orphanet:2557)
Moderate multiminicore disease with hand involvement (Orphanet:178145)
Moebius syndrome (Orphanet:570)
Monosomy 18q (Orphanet:1600)
Monosomy 5p (Orphanet:281)
Monosomy 9p (Orphanet:261112)
Mowat-Wilson syndrome (Orphanet:2152)
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID (OMIM:615575)
Nail-patella syndrome (Orphanet:2614)
Occipital horn syndrome (Orphanet:198)
Oculofaciocardiodental syndrome (Orphanet:2712)
Okihiro syndrome (Orphanet:93293)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Paraplegia - brachydactyly - cone-shaped epiphysis (Orphanet:2823)
Pitt-Hopkins syndrome (Orphanet:2896)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
RETT SYNDROME, CONGENITAL VARIANT (OMIM:613454)
RIENHOFF SYNDROME (OMIM:615582)
RUIJS-AALFS SYNDROME (OMIM:616200)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Richards-Rundle syndrome (Orphanet:1399)
Roussy-Lévy syndrome (Orphanet:3115)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
SATOYOSHI SYNDROME (OMIM:600705)
SECKEL SYNDROME 1 (OMIM:210600)
SMITH-MCCORT DYSPLASIA 2 (OMIM:615222)
SOTOS SYNDROME 1 (OMIM:117550)
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE (OMIM:614066)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 (OMIM:606002)
SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS (OMIM:609616)
STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES (OMIM:612948)
SYMPHALANGISM, PROXIMAL, 1B (OMIM:615298)
Schwartz-Jampel syndrome (Orphanet:800)
Seckel syndrome (Orphanet:808)
Short-rib thoracic dysplasia 5 with or without polydactyly (OMIM:614376)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Smith-Magenis syndrome (Orphanet:819)
Sotos syndrome (Orphanet:821)
Spondylo-ocular syndrome (Orphanet:85194)
Spondylocarpotarsal synostosis (Orphanet:3275)
Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Orphanet:93346)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Spondyloepimetaphyseal dysplasia with multiple dislocations (Orphanet:93360)
Spondyloepiphyseal dysplasia, MacDermot type (Orphanet:163668)
Spondylometaphyseal dysplasia, 'corner fracture' type (Orphanet:93315)
THREE M SYNDROME 1 (OMIM:273750)
TMCO1 defect syndrome (Orphanet:228407)
TRICHORHINOPHALANGEAL SYNDROME, TYPE I (OMIM:190350)
Temtamy syndrome (Orphanet:1777)
Torg-Winchester syndrome (Orphanet:3460)
Townes-Brocks syndrome (Orphanet:857)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Trismus - pseudocamptodactyly (Orphanet:3377)
W syndrome (Orphanet:2804)
Williams syndrome (Orphanet:904)
Wrinkly skin syndrome (Orphanet:2834)
X-linked creatine transporter deficiency (Orphanet:52503)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)
Young adult-onset distal hereditary motor neuropathy (Orphanet:314485)