Overlapping toe

Symptom Information:

Symptom ID: HPO:0001845
Synonyms:
Crossover toe [HPO:0001845]
OVERLAPPING TOES [HPO:0001845]
Overriding toes [HPO:0001845]
Toe clinodactyly [Orphanet:22460]
Overlapping toes [OMIM:Overlapping toes]
Overriding toes [OMIM:Overriding toes]
Clinodactyly of toes [Orphanet:22460]
Overlapping toes (rare) [OMIM:Overlapping toes (rare)]
Quality:
Cross references:
HPO:0001863 "Toe clinodactyly" [Orphanet:22460]
Orphanet:22460 "Clinodactyly of toes" [Orphanet:22460]
OMIM: "Overlapping toes" [OMIM:Overlapping toes]
OMIM: "Overriding toes" [OMIM:Overriding toes]
OMIM: "Overlapping toes (rare)" [OMIM:Overlapping toes (rare)]
Is a (Direct Parents):
Orphanet Abnormality of the foot
HPO         Abnormality of toe
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:
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)