Broad hallux

Symptom Information:

Symptom ID: HPO:0010055
Synonyms:
Abnormally broad great toes [HPO:0010055]
Broad great toe [HPO:0010055]
Broad great toes [HPO:0010055]
Broad great toe [OMIM:Broad great toe]
Broad great toes [OMIM:Broad great toes]
Broad hallux [OMIM:Broad hallux]
Broad/bifid big toe [Orphanet:22540]
Quality:
Cross references:
HPO:0008111 "Broad distal hallux" [Orphanet:22540]
HPO:0010059 "Broad phalanges of the hallux" [Orphanet:22540]
Orphanet:22540 "Broad/bifid big toe" [Orphanet:22540]
OMIM: "Broad great toe" [OMIM:Broad great toe]
OMIM: "Broad great toes" [OMIM:Broad great toes]
OMIM: "Broad hallux" [OMIM:Broad hallux]
Is a (Direct Parents):
HPO         Broad 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 the lower limb(HPO:0002814)
                      Abnormality of the foot(HPO:0001760)
                         Abnormality of toe(HPO:0001780)
                            Broad toe(HPO:0001837)
                               Broad hallux(HPO:0010055)
                            Abnormality of the hallux(HPO:0001844)
                               Broad hallux(HPO:0010055)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of toe(HPO:0001780)
                         Broad toe(HPO:0001837)
                            Broad hallux(HPO:0010055)
                         Abnormality of the hallux(HPO:0001844)
                            Broad hallux(HPO:0010055)
MedDRA:
Database Frequency: 56 / 7739
Resource:

All diseases associated with this symptom:

1q21.1 microdeletion syndrome (Orphanet:250989)
20p12.3 microdeletion syndrome (Orphanet:261295)
2q31.1 microdeletion syndrome (Orphanet:251014)
2q32q33 microdeletion syndrome (Orphanet:251019)
8p23.1 microdeletion syndrome (Orphanet:251071)
Acro-renal-ocular syndrome (Orphanet:959)
Autosomal dominant microcephaly (Orphanet:2514)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Brachydactyly type A2 (Orphanet:93396)
Brachydactyly type B (Orphanet:93383)
CARDIAC MALFORMATION, CLEFT LIP/PALATE, MICROCEPHALY AND DIGITAL ANOMALIES (OMIM:600987)
CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
Cataract - deafness - hypogonadism (Orphanet:1383)
Conotruncal heart malformations (Orphanet:2445)
Craniofrontonasal dysplasia (Orphanet:1520)
EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE (OMIM:615923)
Faciocardiorenal syndrome (Orphanet:1973)
Familial scaphocephaly syndrome, McGillivray type (Orphanet:168624)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2 (OMIM:614749)
Hallux varus - preaxial polysyndactyly (Orphanet:2110)
Heart defect - tongue hamartoma - polysyndactyly (Orphanet:1338)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Intellectual deficit - polydactyly - uncombable hair (Orphanet:3082)
Intellectual deficit, X-linked, Nascimento type (Orphanet:163956)
Jackson-Weiss syndrome (Orphanet:1540)
Jacobsen syndrome (Orphanet:2308)
Keipert syndrome (Orphanet:2662)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Mowat-Wilson syndrome (Orphanet:2152)
Muenke syndrome (Orphanet:53271)
Multiple sulfatase deficiency (Orphanet:585)
Nager syndrome (Orphanet:245)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 1 (Orphanet:90650)
PHAVER syndrome (Orphanet:2876)
Paraplegia - brachydactyly - cone-shaped epiphysis (Orphanet:2823)
Pfeiffer syndrome (Orphanet:710)
Pfeiffer syndrome type 1 (Orphanet:93258)
Pfeiffer syndrome type 2 (Orphanet:93259)
Pfeiffer syndrome type 3 (Orphanet:93260)
Polysyndactyly - cardiac malformation (Orphanet:2934)
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome (Orphanet:276432)
ROBINOW-SORAUF SYNDROME (OMIM:180750)
Rubinstein-Taybi syndrome (Orphanet:783)
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion (Orphanet:353281)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency (Orphanet:353284)
Sakati-Nyhan syndrome (Orphanet:3128)
Split hand-split foot malformation (Orphanet:2440)
Stapes ankylosis with broad thumbs and toes (Orphanet:140917)
TEMPLE-BARAITSER SYNDROME (OMIM:611816)
Townes-Brocks syndrome (Orphanet:857)
Ulna hypoplasia - intellectual deficit (Orphanet:2249)