Toe clinodactyly

Symptom Information:

Symptom ID: HPO:0001863
Synonyms:
Clinodactyly of feet [HPO:0001863]
Clinodactyly of toes [Orphanet:22460]
Quality:
Cross references:
HPO:0001845 "Overlapping toe" [Orphanet:22460]
Orphanet:22460 "Clinodactyly of toes" [Orphanet:22460]
Is a (Direct Parents):
HPO         Abnormality of toe
Orphanet Abnormality of the foot
HPO         Clinodactyly of hallux
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:
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)