2-3 toe syndactyly

Symptom Information:

Symptom ID: HPO:0004691
Synonyms:
2-3 toe soft tissue syndactyly [HPO:0004691]
2-3 toes syndactyly [HPO:0004691]
Complete cutaneous syndactyly of second and third toes [HPO:0004691]
Cutaneous 2,3 toe syndactyly [HPO:0004691]
Cutaneous syndactyly of second and third toes [HPO:0004691]
partial or complete syndactyly 2nd-3rd toes [HPO:0004691]
Syndactyly (2-3) (feet) [HPO:0004691]
Syndactyly of second and third toes [HPO:0004691]
TOE SYNDACTYLY, 2-3 [HPO:0004691]
2-3 toe soft tissue syndactyly [OMIM:2-3 toe soft tissue syndactyly]
2-3 toe syndactyly [OMIM:2-3 toe syndactyly]
Cutaneous 2,3 toe syndactyly [OMIM:Cutaneous 2,3 toe syndactyly]
Cutaneous syndactyly of second and third toes [OMIM:Cutaneous syndactyly of second and third toes]
Syndactyly of second and third toes [OMIM:Syndactyly of second and third toes]
Toe syndactyly, 2-3 [OMIM:Toe syndactyly, 2-3]
Complete cutaneous syndactyly of second and third toes (in some patients) [OMIM:Complete cutaneous syndactyly of second and third toes (in some patients)]
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, toes 2 and 3 [OMIM:Syndactyly, toes 2 and 3]
Syndactyly. [OMIM:Syndactyly.]
Quality:
Cross references:
OMIM: "2-3 toe soft tissue syndactyly" [OMIM:2-3 toe soft tissue syndactyly]
OMIM: "2-3 toe syndactyly" [OMIM:2-3 toe syndactyly]
OMIM: "Cutaneous 2,3 toe syndactyly" [OMIM:Cutaneous 2,3 toe syndactyly]
OMIM: "Cutaneous syndactyly of second and third toes" [OMIM:Cutaneous syndactyly of second and third toes]
OMIM: "Syndactyly of second and third toes" [OMIM:Syndactyly of second and third toes]
OMIM: "Toe syndactyly, 2-3" [OMIM:Toe syndactyly, 2-3]
OMIM: "Complete cutaneous syndactyly of second and third toes (in some patients)" [OMIM:Complete cutaneous syndactyly of second and third toes (in some patients)]
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, toes 2 and 3" [OMIM:Syndactyly, toes 2 and 3]
OMIM: "Syndactyly." [OMIM:Syndactyly.]
Is a (Direct Parents):
HPO         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 the lower limb(HPO:0002814)
                      Abnormality of the foot(HPO:0001760)
                         Abnormality of toe(HPO:0001780)
                            Toe syndactyly(HPO:0001770)
                               2-3 toe syndactyly(HPO:0004691)
                   Abnormality of digit(HPO:0011297)
                      Abnormality of toe(HPO:0001780)
                         Toe syndactyly(HPO:0001770)
                            2-3 toe syndactyly(HPO:0004691)
                      Syndactyly(HPO:0001159)
                         Toe syndactyly(HPO:0001770)
                            2-3 toe syndactyly(HPO:0004691)
MedDRA:
Database Frequency: 50 / 7739
Resource:

All diseases associated with this symptom:

ADAMS-OLIVER SYNDROME 3 (OMIM:614814)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 16 (OMIM:615993)
Brachydactyly type A2 (Orphanet:93396)
CARDIAC MALFORMATION, CLEFT LIP/PALATE, MICROCEPHALY AND DIGITAL ANOMALIES (OMIM:600987)
COLD-INDUCED SWEATING SYNDROME 2 (OMIM:610313)
CORNELIA DE LANGE SYNDROME 4 (OMIM:614701)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Choanal atresia - deafness - cardiac defects - dysmorphism (Orphanet:1200)
Cornelia de Lange syndrome (Orphanet:199)
Corpus callosum agenesis - neuronopathy (Orphanet:1496)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
Craniofrontonasal dysplasia (Orphanet:1520)
Craniosynostosis and dental anomalies (Orphanet:284149)
Craniosynostosis, Philadelphia type (Orphanet:1527)
ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY (OMIM:600906)
Eyebrow duplication - syndactyly (Orphanet:3172)
Faciocardiorenal syndrome (Orphanet:1973)
Feingold syndrome (Orphanet:1305)
Focal dermal hypoplasia (Orphanet:2092)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
HUNTER-MACDONALD SYNDROME (OMIM:611962)
HYDRANENCEPHALY WITH RENAL APLASIA-DYSPLASIA (OMIM:236500)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Hypertelorism-microtia-facial clefting syndrome (Orphanet:2213)
Jackson-Weiss syndrome (Orphanet:1540)
Joubert syndrome 17 (OMIM:614615)
Joubert syndrome 20 (OMIM:614970)
MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
Monosomy 22q13 (Orphanet:48652)
Mulibrey nanism (Orphanet:2576)
Multiple synostoses syndrome (Orphanet:3237)
Myhre syndrome (Orphanet:2588)
Oculofaciocardiodental syndrome (Orphanet:2712)
Pelviscapular dysplasia (Orphanet:93333)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
Saethre-Chotzen syndrome (Orphanet:794)
Scalp-ear-nipple syndrome (Orphanet:2036)
Sialuria (Orphanet:3166)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Symphalangism with multiple anomalies of hands and feet (Orphanet:3246)
Syndactyly type 4 (Orphanet:93405)
Synpolydactyly type 2 (Orphanet:295197)
Timothy syndrome (Orphanet:65283)
Townes-Brocks syndrome (Orphanet:857)
Ulnar/fibula ray defect - brachydactyly (Orphanet:52056)
Warsaw breakage syndrome (Orphanet:280558)