Long hallux

Symptom Information:

Symptom ID: HPO:0001847
Synonyms:
Increased length of the hallux [HPO:0001847]
Large halluces [HPO:0001847]
Long halluces [HPO:0001847]
Large halluces [OMIM:Large halluces]
Long halluces [OMIM:Long halluces]
Long hallux [OMIM:Long hallux]
Long/prehensile big toe [Orphanet:22500]
Large halluces (in some patients) [OMIM:Large halluces (in some patients)]
Quality:
Cross references:
Orphanet:22500 "Long/prehensile big toe" [Orphanet:22500]
OMIM: "Large halluces" [OMIM:Large halluces]
OMIM: "Long halluces" [OMIM:Long halluces]
OMIM: "Long hallux" [OMIM:Long hallux]
OMIM: "Large halluces (in some patients)" [OMIM:Large halluces (in some patients)]
Is a (Direct Parents):
HPO         Long toe
Orphanet Abnormality of the hallux
HPO         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 digit(HPO:0011297)
                      Abnormality of toe(HPO:0001780)
                         Long toe(HPO:0010511)
                            Long hallux(HPO:0001847)
                         Abnormality of the hallux(HPO:0001844)
                            Long hallux(HPO:0001847)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of the foot(HPO:0001760)
                         Abnormality of toe(HPO:0001780)
                            Long toe(HPO:0010511)
                               Long hallux(HPO:0001847)
                            Abnormality of the hallux(HPO:0001844)
                               Long hallux(HPO:0001847)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:101800)
Acrodysostosis with multiple hormone resistance (Orphanet:280651)
Acromesomelic dysplasia, Maroteaux type (Orphanet:40)
CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE (OMIM:615923)
Intellectual deficit, X-linked, Snyder type (Orphanet:3063)
Jacobsen syndrome (Orphanet:2308)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Microcephaly-cardiomyopathy syndrome (Orphanet:2515)
Mowat-Wilson syndrome (Orphanet:2152)
Schilbach-Rott syndrome (Orphanet:2353)
Sialuria (Orphanet:3166)
Van den Ende-Gupta syndrome (Orphanet:2460)