Long hallux
Symptom Information:
Symptom ID: | HPO:0001847 | ||||||||
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) Long hallux(HPO:0001847) Long toe(HPO:0010511) Long hallux(HPO:0001847) Abnormality of the lower limb(HPO:0002814) Abnormality of the foot(HPO:0001760) Abnormality of toe(HPO:0001780) Abnormality of the hallux(HPO:0001844) Long hallux(HPO:0001847) Long toe(HPO:0010511) Long hallux(HPO:0001847) MedDRA: |
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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) |