Broad toe

Symptom Information:

Symptom ID: HPO:0001837
Synonyms:
Broad toes [OMIM:Broad toes]
Broad toes (24%) [OMIM:Broad toes (24%)]
Broad toes (33%) [OMIM:Broad toes (33%)]
Broad toes (rare) [OMIM:Broad toes (rare)]
Quality:
Cross references:
OMIM: "Broad toes" [OMIM:Broad toes]
OMIM: "Broad toes (24%)" [OMIM:Broad toes (24%)]
OMIM: "Broad toes (33%)" [OMIM:Broad toes (33%)]
OMIM: "Broad toes (rare)" [OMIM:Broad toes (rare)]
Is a (Direct Parents):
HPO         Abnormality of toe
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)
                         Abnormality of toe(HPO:0001780)
                            Broad toe(HPO:0001837)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of toe(HPO:0001780)
                         Broad toe(HPO:0001837)
MedDRA:
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)