Preaxial foot polydactyly

Symptom Information:

Symptom ID: HPO:0001841
Synonyms:
Partial/complete duplication of the phalanges of the big toe [HPO:0001841]
Polydactyly affecting the hallux [HPO:0001841]
Preaxial hallucal polydactyly [HPO:0001841]
Preaxial polydactyly (feet) [HPO:0001841]
Preaxial polydactyly of feet [HPO:0001841]
Preaxial polydactyly of foot [HPO:0001841]
Preaxial polydactyly of the feet [HPO:0001841]
Preaxial polydactyly, feet [HPO:0001841]
Preaxial polydactyly of foot [Orphanet:22240]
Preaxial hallucal polydactyly [OMIM:Preaxial hallucal polydactyly]
Preaxial polydactyly of feet [OMIM:Preaxial polydactyly of feet]
Preaxial polydactyly, feet [OMIM:Preaxial polydactyly, feet]
Preaxial polydactyly of toes/big toe duplication [Orphanet:22240]
Polydactyly, preaxial (rare) [OMIM:Polydactyly, preaxial (rare)]
Preaxial polydactyly (rare) [OMIM:Preaxial polydactyly (rare)]
Preaxial polydactyly (variable) [OMIM:Preaxial polydactyly (variable)]
Quality:
Cross references:
Orphanet:22240 "Preaxial polydactyly of toes/big toe duplication" [Orphanet:22240]
OMIM: "Preaxial hallucal polydactyly" [OMIM:Preaxial hallucal polydactyly]
OMIM: "Preaxial polydactyly of feet" [OMIM:Preaxial polydactyly of feet]
OMIM: "Preaxial polydactyly, feet" [OMIM:Preaxial polydactyly, feet]
OMIM: "Polydactyly, preaxial (rare)" [OMIM:Polydactyly, preaxial (rare)]
OMIM: "Preaxial polydactyly (rare)" [OMIM:Preaxial polydactyly (rare)]
OMIM: "Preaxial polydactyly (variable)" [OMIM:Preaxial polydactyly (variable)]
Is a (Direct Parents):
HPO         Preaxial polydactyly
HPO         Foot polydactyly
HPO         Abnormality of the hallux
Orphanet Foot polydactyly
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)
                         Duplication involving bones of the feet(HPO:0009136)
                            Foot polydactyly(HPO:0001829)
                               Preaxial foot polydactyly(HPO:0001841)
                         Abnormality of toe(HPO:0001780)
                            Foot polydactyly(HPO:0001829)
                               Preaxial foot polydactyly(HPO:0001841)
                            Abnormality of the hallux(HPO:0001844)
                               Preaxial foot polydactyly(HPO:0001841)
                   Abnormality of digit(HPO:0011297)
                      Polydactyly(HPO:0010442)
                         Preaxial polydactyly(HPO:0100258)
                            Preaxial foot polydactyly(HPO:0001841)
                         Foot polydactyly(HPO:0001829)
                            Preaxial foot polydactyly(HPO:0001841)
                      Abnormality of toe(HPO:0001780)
                         Foot polydactyly(HPO:0001829)
                            Preaxial foot polydactyly(HPO:0001841)
                         Abnormality of the hallux(HPO:0001844)
                            Preaxial foot polydactyly(HPO:0001841)
MedDRA:
Database Frequency: 24 / 7739
Resource:

All diseases associated with this symptom:

Absent tibia - polydactyly - arachnoid cyst (Orphanet:3328)
Acrocallosal syndrome (Orphanet:36)
Apert syndrome (Orphanet:87)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
CRANIOSYNOSTOSIS WITH ANOMALIES OF THE CRANIAL BASE AND DIGITS (OMIM:218530)
Carpenter syndrome (Orphanet:65759)
Diabetic embryopathy (Orphanet:1926)
Femoral-facial syndrome (Orphanet:1988)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
HIRSCHSPRUNG DISEASE WITH ULNAR POLYDACTYLY, POLYSYNDACTYLY OF BIGTOES, AND VENTRICULAR SEPTAL DEFECT (OMIM:235750)
Jackson-Weiss syndrome (Orphanet:1540)
Joubert syndrome with orofaciodigital defect (Orphanet:2754)
LAMBOTTE SYNDROME (OMIM:245552)
Laurin-Sandrow syndrome (Orphanet:2378)
Mowat-Wilson syndrome (Orphanet:2152)
Multinodular goiter - cystic kidney - polydactyly (Orphanet:2091)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Otopalatodigital syndrome type 2 (Orphanet:90652)
Preaxial polydactyly of toes (Orphanet:295006)
Syndactyly type 2 (Orphanet:93403)
Syndactyly-polydactyly-ear lobe syndrome (Orphanet:3259)
Synpolydactyly type 1 (Orphanet:295195)
Triphalangeal thumb - polysyndactyly syndrome (Orphanet:2950)
Wolf-Hirschhorn syndrome (Orphanet:280)