Short foot

Symptom Information:

Symptom ID: HPO:0001773
Synonyms:
Hypoplastic feet [HPO:0001773]
Short feet [HPO:0001773]
Small feet [HPO:0001773]
Hypoplastic feet [OMIM:Hypoplastic feet]
Short feet [OMIM:Short feet]
Small feet [OMIM:Small feet]
short feet [OMIM:short feet]
Short feet (rare) [OMIM:Short feet (rare)]
Small feet (<10th percentile for height age) [OMIM:Small feet (<10th percentile for height age)]
Small feet (deletion patients) [OMIM:Small feet (deletion patients)]
Small feet (in some patients) [OMIM:Small feet (in some patients)]
Small feet (male and female) [OMIM:Small feet (male and female)]
Short foot/brachydactyly of toes [Orphanet:22040]
Short foot [Orphanet:22040]
Short foot (finding) [Orphanet:22040]
Quality:
Cross references:
Orphanet:22040 "Short foot/brachydactyly of toes" [Orphanet:22040]
OMIM: "Hypoplastic feet" [OMIM:Hypoplastic feet]
OMIM: "Short feet" [OMIM:Short feet]
OMIM: "Small feet" [OMIM:Small feet]
OMIM: "short feet" [OMIM:short feet]
OMIM: "Short feet (rare)" [OMIM:Short feet (rare)]
OMIM: "Small feet (<10th percentile for height age)" [OMIM:Small feet (<10th percentile for height age)]
OMIM: "Small feet (deletion patients)" [OMIM:Small feet (deletion patients)]
OMIM: "Small feet (in some patients)" [OMIM:Small feet (in some patients)]
OMIM: "Small feet (male and female)" [OMIM:Small feet (male and female)]
UMLS:C0576226 "Short foot" [Orphanet:22040]
Is a (Direct Parents):
HPO         Talipes equinovalgus
Orphanet Abnormality of the foot
HPO         Broad foot
HPO         Aplasia/Hypoplasia involving bones of the feet
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)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia of the extremities(HPO:0009815)
                   Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
                      Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
                         Short foot(HPO:0001773)
             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)
                         Broad foot(HPO:0001769)
                            Short foot(HPO:0001773)
                         Positional foot deformity(HPO:0005656)
                            Talipes(HPO:0001883)
                               Talipes equinovalgus(HPO:0001772)
                                  Short foot(HPO:0001773)
                         Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
                            Short foot(HPO:0001773)
                      Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
                         Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
                            Short foot(HPO:0001773)
                   Aplasia/hypoplasia of the extremities(HPO:0009815)
                      Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
                         Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
                            Short foot(HPO:0001773)
MedDRA:
Database Frequency: 86 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
1p36 deletion syndrome (Orphanet:1606)
1q21.1 microdeletion syndrome (Orphanet:250989)
2q23.1 microdeletion syndrome (Orphanet:228402)
2q37 microdeletion syndrome (Orphanet:1001)
3MC SYNDROME 1 (OMIM:257920)
4q21 microdeletion syndrome (Orphanet:238750)
AARSKOG-SCOTT SYNDROME (OMIM:305400)
ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM,AND TRACHEAL STENOSIS (OMIM:601427)
Acro-oto-ocular syndrome (Orphanet:2980)
Acrogeria (Orphanet:2500)
Acromesomelic dysplasia, Grebe type (Orphanet:2098)
Acromesomelic dysplasia, Hunter-Thomson type (Orphanet:968)
Acromicric dysplasia (Orphanet:969)
Atypical Rett syndrome (Orphanet:3095)
Autosomal dominant nonsyndromic intellectual deficit (Orphanet:178469)
Autosomal recessive Kenny-Caffey syndrome (Orphanet:93324)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Autosomal recessive spastic paraplegia type 20 (Orphanet:101000)
Bardet-Biedl syndrome (Orphanet:110)
Bohring-Opitz syndrome (Orphanet:97297)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2 (OMIM:610185)
CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
CONGENITAL DISORDER OF DEGLYCOSYLATION (OMIM:615273)
CORNELIA DE LANGE SYNDROME 2 (OMIM:300590)
CORNELIA DE LANGE SYNDROME 3 (OMIM:610759)
CORNELIA DE LANGE SYNDROME 5 (OMIM:300882)
Cabezas syndrome (Orphanet:85293)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Chondrodysplasia with joint dislocations, gPAPP type (Orphanet:280586)
Dubowitz syndrome (Orphanet:235)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 (OMIM:300672)
FIBROCHONDROGENESIS 1 (OMIM:228520)
Fibrochondrogenesis (Orphanet:2021)
GELEOPHYSIC DYSPLASIA 1 (OMIM:231050)
GELEOPHYSIC DYSPLASIA 2 (OMIM:614185)
Geleophysic dysplasia (Orphanet:2623)
Hallermann-Streiff syndrome (Orphanet:2108)
Hennekam syndrome (Orphanet:2136)
Intellectual deficit - balding - patella luxation - acromicria (Orphanet:3041)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
Intellectual deficit, X-linked, Armfield type (Orphanet:85276)
Intellectual deficit, X-linked, Nascimento type (Orphanet:163956)
Isolated sedoheptulokinase deficiency (ORPHA:440713)
Laurin-Sandrow syndrome (Orphanet:2378)
MENTAL RETARDATION, X-LINKED 91 (OMIM:300577)
MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE (OMIM:616051)
MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES (OMIM:607597)
MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
Mesomelia-synostoses syndrome (Orphanet:2496)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Microcephalic primordial dwarfism, Toriello type (Orphanet:2643)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies (Orphanet:369897)
Multiple synostoses syndrome (Orphanet:3237)
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:257850)
Oculo-palato-cerebral syndrome (Orphanet:2714)
Opsismodysplasia (Orphanet:2746)
Osteoglophonic dwarfism (Orphanet:2645)
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY (OMIM:602342)
Pentasomy X (Orphanet:11)
Peters-plus syndrome (Orphanet:709)
Phocomelia, Schinzel type (Orphanet:2879)
Prader-Willi syndrome (Orphanet:739)
Rett syndrome (Orphanet:778)
Rothmund-Thomson syndrome (Orphanet:2909)
Ruvalcaba syndrome (Orphanet:3121)
SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS (OMIM:609616)
Sanjad-Sakati syndrome (Orphanet:2323)
Schinzel-Giedion syndrome (Orphanet:798)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Short-rib thoracic dysplasia 2 with or without polydactyly (OMIM:611263)
Short-rib thoracic dysplasia 5 with or without polydactyly (OMIM:614376)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Spondyloepiphyseal dysplasia, Cantu type (Orphanet:163654)
Spondyloperipheral dysplasia - short ulna (Orphanet:1856)
Subaortic stenosis - short stature (Orphanet:3191)
Syndactyly - camptodactyly and clinodactyly of fifth fingers - bifid toes (Orphanet:357332)
Syndromic X-linked intellectual deficit due to JARID1C mutation (Orphanet:85279)
TEMPLE SYNDROME (OMIM:616222)
TRICHORHINOPHALANGEAL SYNDROME, TYPE III (OMIM:190351)
Urban-Rogers-Meyer syndrome (Orphanet:3409)
Velo-facial-skeletal syndrome (Orphanet:3424)
Wilson-Turner syndrome (Orphanet:3459)
X-linked spondyloepimetaphyseal dysplasia (Orphanet:93349)
Xq27.3q28 duplication syndrome (Orphanet:261483)