Long toe
Symptom Information:
Symptom ID: | HPO:0010511 | ||||||||
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 the lower limb(HPO:0002814) Abnormality of the foot(HPO:0001760) Abnormality of toe(HPO:0001780) Long toe(HPO:0010511) Abnormality of digit(HPO:0011297) Abnormality of toe(HPO:0001780) Long toe(HPO:0010511) MedDRA: |
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Database Frequency: | 9 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
17q23.1q23.2 microdeletion syndrome | (Orphanet:261279) |
Acute infantile liver failure-multisystemic involvement syndrome | (Orphanet:370088) |
CHROMOSOME 5q12 DELETION SYNDROME | (OMIM:615668) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
Spondylo-ocular syndrome | (Orphanet:85194) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |