Broad distal hallux

Symptom Information:

Symptom ID: HPO:0008111
Synonyms:
Broad hallux [Orphanet:22540]
Broad distal hallux [OMIM:Broad distal hallux]
Broad/bifid big toe [Orphanet:22540]
Broad, distal hallux [OMIM:Broad, distal hallux]
Quality:
Cross references:
HPO:0010059 "Broad phalanges of the hallux" [Orphanet:22540]
HPO:0010055 "Broad hallux" [Orphanet:22540]
Orphanet:22540 "Broad/bifid big toe" [Orphanet:22540]
OMIM: "Broad distal hallux" [OMIM:Broad distal hallux]
OMIM: "Broad, distal hallux" [OMIM:Broad, distal hallux]
Is a (Direct Parents):
HPO         Broad hallux
Orphanet Abnormality of the hallux
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)
                            Abnormality of the hallux(HPO:0001844)
                               Broad hallux(HPO:0010055)
                                  Broad distal hallux(HPO:0008111)
                            Broad toe(HPO:0001837)
                               Broad hallux(HPO:0010055)
                                  Broad distal hallux(HPO:0008111)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of toe(HPO:0001780)
                         Abnormality of the hallux(HPO:0001844)
                            Broad hallux(HPO:0010055)
                               Broad distal hallux(HPO:0008111)
                         Broad toe(HPO:0001837)
                            Broad hallux(HPO:0010055)
                               Broad distal hallux(HPO:0008111)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Apert syndrome (Orphanet:87)
BRACHYDACTYLY, TYPE A1, B (OMIM:607004)
Mowat-Wilson syndrome (Orphanet:2152)