Broad hallux
Symptom Information:
Symptom ID: | HPO:0010055 | |||||||
Synonyms: |
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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) Abnormality of the hallux(HPO:0001844) Broad hallux(HPO:0010055) Broad toe(HPO:0001837) Broad hallux(HPO:0010055) 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 toe(HPO:0001837) Broad hallux(HPO:0010055) MedDRA: |
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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) |