Broad toe
Symptom Information:
Symptom ID: | HPO:0001837 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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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 digit(HPO:0011297) Abnormality of toe(HPO:0001780) Broad toe(HPO:0001837) Abnormality of the lower limb(HPO:0002814) Abnormality of the foot(HPO:0001760) Abnormality of toe(HPO:0001780) Broad toe(HPO:0001837) MedDRA: |
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Database Frequency: | 13 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
17q12 microduplication syndrome | (Orphanet:261272) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Brachydactyly type A6 | (Orphanet:93382) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
Keipert syndrome | (Orphanet:2662) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS | (OMIM:609616) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Subaortic stenosis - short stature | (Orphanet:3191) |
Syndactyly-polydactyly-ear lobe syndrome | (Orphanet:3259) |