Preaxial foot polydactyly
Symptom Information:
Symptom ID: | HPO:0001841 | ||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) Foot polydactyly(HPO:0001829) Preaxial foot polydactyly(HPO:0001841) Preaxial polydactyly(HPO:0100258) 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: |
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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) |