Cutaneous syndactyly of toes

Symptom Information:

Symptom ID: HPO:0010621
Synonyms:
Cutaneous syndactyly (feet) [HPO:0010621]
soft tissue syndactyly of toes [HPO:0010621]
Syndactyly, cutaneous (feet) [HPO:0010621]
Syndactyly of toes (disorder) [Orphanet:22340]
Soft tissue syndactyly of toes [OMIM:Soft tissue syndactyly of toes]
Syndactyly of toes [Orphanet:22340]
Toes webbed [Orphanet:22340]
Syndactyly [MedDRA:10042778]
Fingers webbed [MedDRA:10042778]
Fusion of 2nd &
3rd toes both sides [MedDRA:10042778]
Syndactyly of fingers with fusion of bone [MedDRA:10042778]
Syndactyly of fingers without fusion of bone [MedDRA:10042778]
Syndactyly of multiple and unspecified sites [MedDRA:10042778]
Syndactyly of toes with fusion of bone [MedDRA:10042778]
Syndactyly of toes without fusion of bone [MedDRA:10042778]
Toes webbed [MedDRA:10042778]
Web bad fingers [MedDRA:10042778]
Webbed fingers [MedDRA:10042778]
Webbing &
fusion 2-4th fingers L hand [MedDRA:10042778]
Polysyndactyly [MedDRA:10042778]
Cutaneous syndactyly (2,3,4) [OMIM:Cutaneous syndactyly (2,3,4)]
Cutaneous syndactyly (2nd-3rd, 4th-5th) [OMIM:Cutaneous syndactyly (2nd-3rd, 4th-5th)]
Cutaneous syndactyly (digits 2nd-5th) [OMIM:Cutaneous syndactyly (digits 2nd-5th)]
Cutaneous syndactyly (fingers 2,3,4,5) [OMIM:Cutaneous syndactyly (fingers 2,3,4,5)]
Cutaneous syndactyly (in some patients) [OMIM:Cutaneous syndactyly (in some patients)]
Cutaneous syndactyly (less common) [OMIM:Cutaneous syndactyly (less common)]
Cutaneous syndactyly (toes 2-3) [OMIM:Cutaneous syndactyly (toes 2-3)]
Cutaneous syndactyly of toes (in some patients) [OMIM:Cutaneous syndactyly of toes (in some patients)]
Polysyndactyly [OMIM:Polysyndactyly]
Syndactyly (2-3 toe) [OMIM:Syndactyly (2-3 toe)]
Syndactyly (2-3) [OMIM:Syndactyly (2-3)]
Syndactyly (2-3, 4-5) [OMIM:Syndactyly (2-3, 4-5)]
Syndactyly (2nd, 3rd, 4th digits) [OMIM:Syndactyly (2nd, 3rd, 4th digits)]
Syndactyly (2nd-5th toes) [OMIM:Syndactyly (2nd-5th toes)]
Syndactyly (3-4 finger) [OMIM:Syndactyly (3-4 finger)]
Syndactyly (4-5 toes) [OMIM:Syndactyly (4-5 toes)]
Syndactyly (75%) [OMIM:Syndactyly (75%)]
Syndactyly (females) [OMIM:Syndactyly (females)]
Syndactyly (fingers 3-4) [OMIM:Syndactyly (fingers 3-4)]
Syndactyly (in some patients) [OMIM:Syndactyly (in some patients)]
Syndactyly (in some) [OMIM:Syndactyly (in some)]
Syndactyly (often 3rd and 4th digits) [OMIM:Syndactyly (often 3rd and 4th digits)]
Syndactyly (often 3rd-4th toes) [OMIM:Syndactyly (often 3rd-4th toes)]
Syndactyly (rare) [OMIM:Syndactyly (rare)]
Syndactyly (toes 2-3) [OMIM:Syndactyly (toes 2-3)]
Syndactyly (usually fingers 3 and 4) [OMIM:Syndactyly (usually fingers 3 and 4)]
Syndactyly (usually toes 1 to 3) [OMIM:Syndactyly (usually toes 1 to 3)]
Syndactyly of toes (in some patients) [OMIM:Syndactyly of toes (in some patients)]
Syndactyly. [OMIM:Syndactyly.]
Webbed fingers [OMIM:Webbed fingers]
Quality:
Cross references:
Orphanet:22340 "Syndactyly of toes" [Orphanet:22340]
OMIM: "Soft tissue syndactyly of toes" [OMIM:Soft tissue syndactyly of toes]
OMIM: "Cutaneous syndactyly (2,3,4)" [OMIM:Cutaneous syndactyly (2,3,4)]
OMIM: "Cutaneous syndactyly (2nd-3rd, 4th-5th)" [OMIM:Cutaneous syndactyly (2nd-3rd, 4th-5th)]
OMIM: "Cutaneous syndactyly (digits 2nd-5th)" [OMIM:Cutaneous syndactyly (digits 2nd-5th)]
OMIM: "Cutaneous syndactyly (fingers 2,3,4,5)" [OMIM:Cutaneous syndactyly (fingers 2,3,4,5)]
OMIM: "Cutaneous syndactyly (in some patients)" [OMIM:Cutaneous syndactyly (in some patients)]
OMIM: "Cutaneous syndactyly (less common)" [OMIM:Cutaneous syndactyly (less common)]
OMIM: "Cutaneous syndactyly (toes 2-3)" [OMIM:Cutaneous syndactyly (toes 2-3)]
OMIM: "Cutaneous syndactyly of toes (in some patients)" [OMIM:Cutaneous syndactyly of toes (in some patients)]
OMIM: "Polysyndactyly" [OMIM:Polysyndactyly]
OMIM: "Syndactyly (2-3 toe)" [OMIM:Syndactyly (2-3 toe)]
OMIM: "Syndactyly (2-3)" [OMIM:Syndactyly (2-3)]
OMIM: "Syndactyly (2-3, 4-5)" [OMIM:Syndactyly (2-3, 4-5)]
OMIM: "Syndactyly (2nd, 3rd, 4th digits)" [OMIM:Syndactyly (2nd, 3rd, 4th digits)]
OMIM: "Syndactyly (2nd-5th toes)" [OMIM:Syndactyly (2nd-5th toes)]
OMIM: "Syndactyly (3-4 finger)" [OMIM:Syndactyly (3-4 finger)]
OMIM: "Syndactyly (4-5 toes)" [OMIM:Syndactyly (4-5 toes)]
OMIM: "Syndactyly (75%)" [OMIM:Syndactyly (75%)]
OMIM: "Syndactyly (females)" [OMIM:Syndactyly (females)]
OMIM: "Syndactyly (fingers 3-4)" [OMIM:Syndactyly (fingers 3-4)]
OMIM: "Syndactyly (in some patients)" [OMIM:Syndactyly (in some patients)]
OMIM: "Syndactyly (in some)" [OMIM:Syndactyly (in some)]
OMIM: "Syndactyly (often 3rd and 4th digits)" [OMIM:Syndactyly (often 3rd and 4th digits)]
OMIM: "Syndactyly (often 3rd-4th toes)" [OMIM:Syndactyly (often 3rd-4th toes)]
OMIM: "Syndactyly (rare)" [OMIM:Syndactyly (rare)]
OMIM: "Syndactyly (toes 2-3)" [OMIM:Syndactyly (toes 2-3)]
OMIM: "Syndactyly (usually fingers 3 and 4)" [OMIM:Syndactyly (usually fingers 3 and 4)]
OMIM: "Syndactyly (usually toes 1 to 3)" [OMIM:Syndactyly (usually toes 1 to 3)]
OMIM: "Syndactyly of toes (in some patients)" [OMIM:Syndactyly of toes (in some patients)]
OMIM: "Syndactyly." [OMIM:Syndactyly.]
OMIM: "Webbed fingers" [OMIM:Webbed fingers]
Is a (Direct Parents):
Orphanet Abnormality of the foot
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
HPO         Toe syndactyly
Orphanet Toe syndactyly
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 syndactyly(HPO:0001770)
                            Cutaneous syndactyly of toes(HPO:0010621)
                      Syndactyly(HPO:0001159)
                         Toe syndactyly(HPO:0001770)
                            Cutaneous syndactyly of toes(HPO:0010621)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of the foot(HPO:0001760)
                         Abnormality of toe(HPO:0001780)
                            Toe syndactyly(HPO:0001770)
                               Cutaneous syndactyly of toes(HPO:0010621)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396)
       Musculoskeletal and connective tissue disorders of limbs congenital(MedDRA:10028381)
          Cutaneous syndactyly of toes(HPO:0010621)
Database Frequency: 36 / 7739
Resource:

All diseases associated with this symptom:

Absence of fingerprints - congenital milia (Orphanet:1658)
Blepharophimosis - ptosis - esotropia - syndactyly - short stature (Orphanet:2057)
Brachydactyly type A2 (Orphanet:93396)
Brachydactyly type B (Orphanet:93383)
Brachydactyly type B2 (Orphanet:140908)
CORNELIA DE LANGE SYNDROME 4 (OMIM:614701)
CREE MENTAL RETARDATION SYNDROME (OMIM:606851)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Cranioectodermal dysplasia 4 (OMIM:614378)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
Craniofrontonasal dysplasia (Orphanet:1520)
Craniosynostosis and dental anomalies (Orphanet:284149)
Curry-Jones syndrome (Orphanet:1553)
Deafness - onychodystrophy, autosomal dominant (Orphanet:79499)
Faciocardiorenal syndrome (Orphanet:1973)
Focal dermal hypoplasia (Orphanet:2092)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
Hennekam syndrome (Orphanet:2136)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Joubert syndrome 17 (OMIM:614615)
Joubert syndrome 20 (OMIM:614970)
MEIER-GORLIN SYNDROME 1 (OMIM:224690)
MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
POLYDACTYLY, POSTAXIAL, TYPE A5 (OMIM:263450)
Pelviscapular dysplasia (Orphanet:93333)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Rosselli-Gulienetti syndrome (Orphanet:90339)
SHORT RIB-POLYDACTYLY SYNDROME, TYPE IIB (OMIM:615087)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
Saethre-Chotzen syndrome (Orphanet:794)
Symphalangism with multiple anomalies of hands and feet (Orphanet:3246)
Synpolydactyly type 2 (Orphanet:295197)
Timothy syndrome (Orphanet:65283)
Trismus - pseudocamptodactyly (Orphanet:3377)
Ulnar/fibula ray defect - brachydactyly (Orphanet:52056)
Zlotogora-Ogur syndrome (Orphanet:3253)