Foot polydactyly
Symptom Information:
Symptom ID: | HPO:0001829 | |||||||||||||||||
Synonyms: |
|
|||||||||||||||||
Quality: | ||||||||||||||||||
Cross references: |
|
|||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||
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) Abnormality of toe(HPO:0001780) Foot polydactyly(HPO:0001829) Abnormality of digit(HPO:0011297) Polydactyly(HPO:0010442) Foot polydactyly(HPO:0001829) Abnormality of toe(HPO:0001780) Foot polydactyly(HPO:0001829) MedDRA: 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 | |||||||||||||||||
Resource: |
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) |
PELGER-HUET ANOMALY | (OMIM:169400) |
Syndactyly type 4 | (Orphanet:93405) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |