Toe clinodactyly
Symptom Information:
Symptom ID: | HPO:0001863 | ||||||
Synonyms: |
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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) Toe clinodactyly(HPO:0001863) Abnormality of the lower limb(HPO:0002814) Abnormality of the foot(HPO:0001760) Abnormality of toe(HPO:0001780) Toe clinodactyly(HPO:0001863) MedDRA: |
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Database Frequency: | 12 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
14q11.2 microdeletion syndrome | (Orphanet:261120) |
19p13.12 microdeletion syndrome | (Orphanet:254346) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
2q32q33 microdeletion syndrome | (Orphanet:251019) |
AGONADISM, 46,XY, WITH MENTAL RETARDATION, SHORT STATURE, RETARDEDBONE AGE, AND MULTIPLE EXTRAGENITAL MALFORMATIONS | (OMIM:600908) |
CHARGE syndrome | (Orphanet:138) |
DESBUQUOIS DYSPLASIA 2 | (OMIM:615777) |
Jacobsen syndrome | (Orphanet:2308) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Microcephaly - intellectual deficit - phalangeal and neurological anomalies | (Orphanet:137658) |
Suarez-Stickler syndrome | (Orphanet:166277) |
Terminal osseous dysplasia - pigmentary defects | (Orphanet:88630) |