Foot polydactyly

Symptom Information:

Symptom ID: HPO:0001829
Duplication of bones of the toes [HPO:0001829]
Polydactyly (feet) [HPO:0001829]
Polydactyly of foot [Orphanet:22220]
Polydactyly of toes (disorder) [Orphanet:22220]
Polydactyly of toes [Orphanet:22220]
Polydactyly [MedDRA:10036063]
Multiple digits [MedDRA:10036063]
Polydactyly of fingers [MedDRA:10036063]
Polydactyly of toes [MedDRA:10036063]
Polydactyly, unspecified digits [MedDRA:10036063]
Polydactyly (homozygote) [OMIM:Polydactyly (homozygote)]
Polydactyly (in 1 patient) [OMIM:Polydactyly (in 1 patient)]
Polydactyly (in some patients) [OMIM:Polydactyly (in some patients)]
Polydactyly (in some) [OMIM:Polydactyly (in some)]
Polydactyly (major) [OMIM:Polydactyly (major)]
Polydactyly (rare) [OMIM:Polydactyly (rare)]
Polydactyly (variable) [OMIM:Polydactyly (variable)]
Cross references:
Orphanet:22220 "Polydactyly of toes" [Orphanet:22220]
OMIM: "Polydactyly (homozygote)" [OMIM:Polydactyly (homozygote)]
OMIM: "Polydactyly (in 1 patient)" [OMIM:Polydactyly (in 1 patient)]
OMIM: "Polydactyly (in some patients)" [OMIM:Polydactyly (in some patients)]
OMIM: "Polydactyly (in some)" [OMIM:Polydactyly (in some)]
OMIM: "Polydactyly (major)" [OMIM:Polydactyly (major)]
OMIM: "Polydactyly (rare)" [OMIM:Polydactyly (rare)]
OMIM: "Polydactyly (variable)" [OMIM:Polydactyly (variable)]
UMLS:C0158734 "Polydactyly of toes" [Orphanet:22220]
Is a (Direct Parents):
HPO         Duplication involving bones of the feet
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
HPO         Polydactyly
HPO         Abnormality of toe
Orphanet Abnormality of the foot
Is a (Whole tree): HPO:
    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)
                         Abnormality of toe(HPO:0001780)
                            Foot polydactyly(HPO:0001829)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of toe(HPO:0001780)
                         Foot polydactyly(HPO:0001829)
                         Foot polydactyly(HPO:0001829)
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)
          Foot polydactyly(HPO:0001829)
Database Frequency: 41 / 7739

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
1q21.1 microdeletion syndrome (Orphanet:250989)
22q11.2 deletion syndrome (Orphanet:567)
Acro-cardio-facial syndrome (Orphanet:2008)
Acro-renal-mandibular syndrome (Orphanet:958)
Acrocephalopolydactyly (Orphanet:221054)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 4 (OMIM:615982)
Bardet-Biedl syndrome 7 (OMIM:615984)
Bardet-Biedl syndrome 9 (OMIM:615986)
Char syndrome (Orphanet:46627)
Curry-Jones syndrome (Orphanet:1553)
Diabetic embryopathy (Orphanet:1926)
Ellis Van Creveld syndrome (Orphanet:289)
Familial clubfoot with or without associated lower limb anomalies (Orphanet:199315)
Focal dermal hypoplasia (Orphanet:2092)
Harlequin ichthyosis (Orphanet:457)
Hirschsprung disease - deafness - polydactyly (Orphanet:2155)
Holoprosencephaly - radial heart renal anomalies (Orphanet:3186)
Jeune syndrome (Orphanet:474)
Joubert syndrome (Orphanet:475)
Joubert syndrome 15 (OMIM:614464)
Joubert syndrome 16 (OMIM:614465)
Joubert syndrome 17 (OMIM:614615)
Joubert syndrome with ocular defect (Orphanet:220493)
Joubert syndrome with oculorenal defect (Orphanet:2318)
Joubert syndrome with orofaciodigital defect (Orphanet:2754)
Juvenile polyposis syndrome (Orphanet:2929)
Lhermitte-Duclos disease (Orphanet:65285)
Meckel syndrome (Orphanet:564)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Mirror polydactyly - vertebral segmentation - limbs defects (Orphanet:3004)
Mycophenolate mofetil embryopathy (Orphanet:268249)
Nephronophthisis 15 (OMIM:614845)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Syndactyly type 4 (Orphanet:93405)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)