Pes planus
Symptom Information:
Symptom ID: | HPO:0001763 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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 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 deformities (incl intervertebral disc disorders)(MedDRA:10028377) Extremity deformities(MedDRA:10012139) Pes planus(HPO:0001763) Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396) Musculoskeletal and connective tissue disorders of limbs congenital(MedDRA:10028381) Pes planus(HPO:0001763) |
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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) |