Overlapping toe
Symptom Information:
Symptom ID: | HPO:0001845 | ||||||||
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) Overlapping toe(HPO:0001845) Abnormality of digit(HPO:0011297) Abnormality of toe(HPO:0001780) Overlapping toe(HPO:0001845) MedDRA: |
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Database Frequency: | 18 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
19q13.11 microdeletion syndrome | (Orphanet:217346) |
ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY | (OMIM:614262) |
Acrofacial dysostosis, Rodriguez type | (Orphanet:1788) |
Bohring-Opitz syndrome | (Orphanet:97297) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
FRASER-LIKE SYNDROME | (OMIM:229230) |
Gordon syndrome | (Orphanet:376) |
MELAS | (Orphanet:550) |
Micrencephaly - corpus callosum agenesis - abnormal genitalia | (Orphanet:2508) |
Micro syndrome | (Orphanet:2510) |
Monosomy 18q | (Orphanet:1600) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Myhre syndrome | (Orphanet:2588) |
Nager syndrome | (Orphanet:245) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
WARBURG MICRO SYNDROME 1 | (OMIM:600118) |
WARBURG MICRO SYNDROME 2 | (OMIM:614225) |
Weaver syndrome | (Orphanet:3447) |