Overlapping fingers

Symptom Information:

Symptom ID: HPO:0010557
Synonyms:
Overlapping fingers [OMIM:Overlapping fingers]
Clinodactyly of fingers 1,2,3,4/overlapping fingers [Orphanet:20640]
First finger clinodactyly [Orphanet:20640]
Fourth finger Clinodactyly [Orphanet:20640]
Third finger clinodactyly [Orphanet:20640]
Quality:
Cross references:
Orphanet:20640 "Clinodactyly of fingers 1,2,3,4/overlapping fingers" [Orphanet:20640]
OMIM: "Overlapping fingers" [OMIM:Overlapping fingers]
Is a (Direct Parents):
Orphanet Radial deviation of the 2nd finger
HPO         Deviation of finger
Orphanet Abnormality of the hand
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 finger(HPO:0001167)
                         Deviation of finger(HPO:0004097)
                            Overlapping fingers(HPO:0010557)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of finger(HPO:0001167)
                            Deviation of finger(HPO:0004097)
                               Overlapping fingers(HPO:0010557)
                         Deviation of the hand or of fingers of the hand(HPO:0009484)
                            Deviation of finger(HPO:0004097)
                               Overlapping fingers(HPO:0010557)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Bangstad syndrome (Orphanet:1227)
Congenital lethal myopathy, Compton-North type (Orphanet:210163)
Fetal Gaucher disease (Orphanet:85212)
GCS1-CDG (Orphanet:79330)
IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES (OMIM:615966)
Kapur-Toriello syndrome (Orphanet:2328)
MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM (OMIM:601016)
Otopalatodigital syndrome (Orphanet:669)
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis (Orphanet:65288)