Short toe

Symptom Information:

Symptom ID: HPO:0001831
Synonyms:
Brachydactyly of the foot [HPO:0001831]
Hypoplasia of the toe [HPO:0001831]
Hypoplastic or dysplastic toes [HPO:0001831]
Hypoplastic toes [HPO:0001831]
Short phalanges (feet) [HPO:0001831]
Short toes [HPO:0001831]
Hypoplastic toes [OMIM:Hypoplastic toes]
Short toes [OMIM:Short toes]
Short foot/brachydactyly of toes [Orphanet:22040]
Hypoplastic or dysplastic toes (3rd, 4th, and 5th) [OMIM:Hypoplastic or dysplastic toes (3rd, 4th, and 5th)]
Hypoplastic toes (in some cases) [OMIM:Hypoplastic toes (in some cases)]
Hypoplastic toes (in some patients) [OMIM:Hypoplastic toes (in some patients)]
Hypoplastic toes (rare) [OMIM:Hypoplastic toes (rare)]
Short phalanges (especially distal phalanges) [OMIM:Short phalanges (especially distal phalanges)]
Short phalanges (middle phalanges) [OMIM:Short phalanges (middle phalanges)]
Short phalanges (rare) [OMIM:Short phalanges (rare)]
Short toes (2nd-5th) [OMIM:Short toes (2nd-5th)]
Short foot [Orphanet:22040]
Short foot (finding) [Orphanet:22040]
Quality:
Cross references:
Orphanet:22040 "Short foot/brachydactyly of toes" [Orphanet:22040]
OMIM: "Hypoplastic toes" [OMIM:Hypoplastic toes]
OMIM: "Short toes" [OMIM:Short toes]
OMIM: "Hypoplastic or dysplastic toes (3rd, 4th, and 5th)" [OMIM:Hypoplastic or dysplastic toes (3rd, 4th, and 5th)]
OMIM: "Hypoplastic toes (in some cases)" [OMIM:Hypoplastic toes (in some cases)]
OMIM: "Hypoplastic toes (in some patients)" [OMIM:Hypoplastic toes (in some patients)]
OMIM: "Hypoplastic toes (rare)" [OMIM:Hypoplastic toes (rare)]
OMIM: "Short phalanges (especially distal phalanges)" [OMIM:Short phalanges (especially distal phalanges)]
OMIM: "Short phalanges (middle phalanges)" [OMIM:Short phalanges (middle phalanges)]
OMIM: "Short phalanges (rare)" [OMIM:Short phalanges (rare)]
OMIM: "Short toes (2nd-5th)" [OMIM:Short toes (2nd-5th)]
UMLS:C0576226 "Short foot" [Orphanet:22040]
Is a (Direct Parents):
HPO         Short digit
HPO         Aplasia/Hypoplasia of toe
Orphanet Short foot
Orphanet Abnormality of the foot
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 digit(HPO:0011297)
                      Abnormality of toe(HPO:0001780)
                         Aplasia/Hypoplasia of toe(HPO:0001991)
                            Short toe(HPO:0001831)
                      Short digit(HPO:0011927)
                         Short toe(HPO:0001831)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of the foot(HPO:0001760)
                         Abnormality of toe(HPO:0001780)
                            Aplasia/Hypoplasia of toe(HPO:0001991)
                               Short toe(HPO:0001831)
                         Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
                            Aplasia/Hypoplasia of toe(HPO:0001991)
                               Short toe(HPO:0001831)
                      Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
                         Aplasia/Hypoplasia involving bones of the feet(HPO:0006494)
                            Aplasia/Hypoplasia of toe(HPO:0001991)
                               Short toe(HPO:0001831)
                   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)
                            Aplasia/Hypoplasia of toe(HPO:0001991)
                               Short toe(HPO:0001831)
             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)
                         Aplasia/Hypoplasia of toe(HPO:0001991)
                            Short toe(HPO:0001831)
MedDRA:
Database Frequency: 52 / 7739
Resource:

All diseases associated with this symptom:

16p13.3 microduplication syndrome (Orphanet:96078)
2q37 microdeletion syndrome (Orphanet:1001)
ADAMS-OLIVER SYNDROME 4 (OMIM:615297)
Acromesomelic dysplasia, Maroteaux type (Orphanet:40)
Albright hereditary osteodystrophy (Orphanet:665)
Alström syndrome (Orphanet:64)
Anauxetic dysplasia (Orphanet:93347)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
Bohring-Opitz syndrome (Orphanet:97297)
Borjeson-Forssman-Lehmann syndrome (Orphanet:127)
Brachydactyly type A6 (Orphanet:93382)
CHONDRODYSPLASIA, ACROMESOMELIC, WITH GENITAL ANOMALIES (OMIM:609441)
Camptobrachydactyly (Orphanet:1319)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Chondrodysplasia with joint dislocations, gPAPP type (Orphanet:280586)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Craniosynostosis and dental anomalies (Orphanet:284149)
Czech dysplasia, metatarsal type (Orphanet:137678)
Ehlers-Danlos syndrome, dermatosparaxis type (Orphanet:1901)
FEINGOLD SYNDROME 1 (OMIM:164280)
Feingold syndrome (Orphanet:1305)
HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS (OMIM:610680)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 (OMIM:239300)
Hyperphosphatasia-intellectual deficiency syndrome (Orphanet:247262)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2 (OMIM:242100)
Intellectual deficit, X-linked, Vitale type (Orphanet:85289)
Keipert syndrome (Orphanet:2662)
Léri-Weill dyschondrosteosis (Orphanet:240)
MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUALAPPEARANCE (OMIM:612947)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Metaphyseal chondrodysplasia, Kaitila type (Orphanet:166038)
Microcephaly-capillary malformation syndrome (Orphanet:294016)
Myhre syndrome (Orphanet:2588)
Nager syndrome (Orphanet:245)
OSTEODYSPLASTY, PRECOCIOUS, OF DANKS, MAYNE, AND KOZLOWSKI (OMIM:259270)
Oculoosteocutaneous syndrome (Orphanet:2713)
Paraplegia - brachydactyly - cone-shaped epiphysis (Orphanet:2823)
Patent ductus arteriosus - bicuspid aortic valve - hand anomalies (Orphanet:228190)
Self-healing collodion baby (Orphanet:281122)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Spondyloepiphyseal dysplasia, Cantu type (Orphanet:163654)
Spondylometaphyseal dysplasia, Sedaghatian type (Orphanet:93317)
Spondyloperipheral dysplasia - short ulna (Orphanet:1856)
Subaortic stenosis - short stature (Orphanet:3191)
THAI SYMPHALANGISM SYNDROME (OMIM:608028)
Terminal osseous dysplasia - pigmentary defects (Orphanet:88630)
Tetrasomy 12p (Orphanet:884)
Tricho-retino-dento-digital syndrome (Orphanet:1264)
Wiedemann-Steiner syndrome (Orphanet:319182)
Yunis-Varon syndrome (Orphanet:3472)