Toe syndactyly

Symptom Information:

Symptom ID: HPO:0001770
Synonyms:
Syndactyly (feet) [HPO:0001770]
Syndactyly of toes [HPO:0001770]
Syndactyly of toes [OMIM:Syndactyly of toes]
Toe syndactyly [OMIM:Toe syndactyly]
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.]
Syndactyly of toes [Orphanet:22340]
Quality:
Cross references:
Orphanet:22340 "Syndactyly of toes" [Orphanet:22340]
OMIM: "Syndactyly of toes" [OMIM:Syndactyly of toes]
OMIM: "Toe syndactyly" [OMIM:Toe syndactyly]
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.]
Is a (Direct Parents):
HPO         Abnormality of toe
HPO         Syndactyly
Orphanet Abnormality of the foot
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)
                      Syndactyly(HPO:0001159)
                         Toe syndactyly(HPO:0001770)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of the foot(HPO:0001760)
                         Abnormality of toe(HPO:0001780)
                            Toe syndactyly(HPO:0001770)
MedDRA:
Database Frequency: 149 / 7739
Resource:

All diseases associated with this symptom:

14q11.2 microdeletion syndrome (Orphanet:261120)
14q22q23 microdeletion syndrome (Orphanet:264200)
15q24 microdeletion syndrome (Orphanet:94065)
16p11.2p12.2 microdeletion syndrome (Orphanet:261211)
17q12 microduplication syndrome (Orphanet:261272)
17q21.31 microduplication syndrome (Orphanet:217340)
19q13.11 microdeletion syndrome (Orphanet:217346)
1q21.1 microdeletion syndrome (Orphanet:250989)
2q31.1 microdeletion syndrome (Orphanet:251014)
2q37 microdeletion syndrome (Orphanet:1001)
3C syndrome (Orphanet:7)
3q29 microduplication (Orphanet:251038)
4q21 microdeletion syndrome (Orphanet:238750)
5q14.3 microdeletion syndrome (Orphanet:228384)
8p23.1 microduplication syndrome (Orphanet:251076)
ADULT syndrome (Orphanet:978)
AGONADISM, 46,XY, WITH MENTAL RETARDATION, SHORT STATURE, RETARDEDBONE AGE, AND MULTIPLE EXTRAGENITAL MALFORMATIONS (OMIM:600908)
Ablepharon macrostomia syndrome (Orphanet:920)
Abruzzo-Erickson syndrome (Orphanet:921)
Absent tibia - polydactyly - arachnoid cyst (Orphanet:3328)
Acro-cardio-facial syndrome (Orphanet:2008)
Acro-oto-ocular syndrome (Orphanet:2980)
Acro-renal-mandibular syndrome (Orphanet:958)
Acro-renal-ocular syndrome (Orphanet:959)
Acrocallosal syndrome (Orphanet:36)
Acropectorovertebral dysplasia (Orphanet:957)
Adams-Oliver syndrome (Orphanet:974)
Apert syndrome (Orphanet:87)
Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis (Orphanet:1112)
Aphalangy - syndactyly - microcephaly (Orphanet:1113)
Autosomal dominant popliteal pterygium syndrome (Orphanet:1300)
Autosomal recessive Robinow syndrome (Orphanet:1507)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
Bartsocas-Papas syndrome (Orphanet:1234)
Brachydactyly type A2 (Orphanet:93396)
Brachydactyly-syndactyly, Zhao type (Orphanet:93409)
C syndrome (Orphanet:1308)
CORNELIA DE LANGE SYNDROME 4 (OMIM:614701)
CORNELIA DE LANGE SYNDROME 5 (OMIM:300882)
Cabezas syndrome (Orphanet:85293)
Camptobrachydactyly (Orphanet:1319)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Carpenter syndrome (Orphanet:65759)
Cenani-Lenz syndrome (Orphanet:3258)
Char syndrome (Orphanet:46627)
Cornelia de Lange syndrome (Orphanet:199)
Crane-Heise syndrome (Orphanet:1512)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
Craniofrontonasal dysplasia (Orphanet:1520)
Craniomicromelic syndrome (Orphanet:1524)
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis (Orphanet:171839)
Craniosynostosis and dental anomalies (Orphanet:284149)
Curry-Jones syndrome (Orphanet:1553)
Cutis marmorata telangiectatica congenita (Orphanet:1556)
Deafness - genital anomalies - metacarpal and metatarsal synostosis (Orphanet:3224)
Deafness - onychodystrophy (Orphanet:3231)
Deafness - onychodystrophy, autosomal dominant (Orphanet:79499)
Diaphragmatic defect - limb deficiency - skull defect (Orphanet:2141)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal 22q11.2 microduplication syndrome (Orphanet:261337)
Distal monosomy 10q (Orphanet:96148)
Dubowitz syndrome (Orphanet:235)
Dystrophic epidermolysis bullosa (Orphanet:303)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
Ermine phenotype (Orphanet:999)
Faciocardiorenal syndrome (Orphanet:1973)
Fallot complex - intellectual deficit - growth delay (Orphanet:3304)
Familial scaphocephaly syndrome, McGillivray type (Orphanet:168624)
Fanconi anemia (Orphanet:84)
Feingold syndrome (Orphanet:1305)
Femoral-facial syndrome (Orphanet:1988)
Focal dermal hypoplasia (Orphanet:2092)
Fraser syndrome (Orphanet:2052)
Fuhrmann syndrome (Orphanet:2854)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Intellectual deficit - balding - patella luxation - acromicria (Orphanet:3041)
Intellectual deficit - polydactyly - uncombable hair (Orphanet:3082)
Jackson-Weiss syndrome (Orphanet:1540)
Jacobsen syndrome (Orphanet:2308)
Jeune syndrome (Orphanet:474)
Joubert syndrome 17 (OMIM:614615)
Joubert syndrome 20 (OMIM:614970)
Joubert syndrome with orofaciodigital defect (Orphanet:2754)
Juberg-Hayward syndrome (Orphanet:2319)
Junctional epidermolysis bullosa (Orphanet:305)
Junctional epidermolysis bullosa, Herlitz type (Orphanet:79404)
Lathosterolosis (Orphanet:46059)
Laurin-Sandrow syndrome (Orphanet:2378)
Linear verrucous nevus syndrome (Orphanet:2611)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Mesoaxial synostotic syndactyly with phalangeal reduction (Orphanet:157801)
Microduplication Xp11.22-p11.23 syndrome (Orphanet:217377)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Microphthalmia with limb anomalies (Orphanet:1106)
Monosomy 18q (Orphanet:1600)
Mowat-Wilson syndrome (Orphanet:2152)
Nager syndrome (Orphanet:245)
Neu-Laxova syndrome (Orphanet:2671)
Nevus comedonicus syndrome (Orphanet:64754)
Oculodentodigital dysplasia (Orphanet:2710)
Oculofaciocardiodental syndrome (Orphanet:2712)
Odontotrichomelic syndrome (Orphanet:2723)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Orofaciodigital syndrome type 9 (Orphanet:141007)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 1 (Orphanet:90650)
Pallister-Hall syndrome (Orphanet:672)
Patterson-Stevenson-Fontaine syndrome (Orphanet:2439)
Pelvis-shoulder dysplasia (Orphanet:2839)
Pelviscapular dysplasia (Orphanet:93333)
Peters-plus syndrome (Orphanet:709)
Pfeiffer syndrome type 1 (Orphanet:93258)
Pfeiffer syndrome type 2 (Orphanet:93259)
Pfeiffer syndrome type 3 (Orphanet:93260)
Polysyndactyly - cardiac malformation (Orphanet:2934)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Recessive aplasia cutis congenita of limbs (Orphanet:1115)
Recessive dystrophic epidermolysis bullosa-generalized other (Orphanet:89842)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
SPLIT-HAND/FOOT MALFORMATION 6 (OMIM:225300)
Saethre-Chotzen syndrome (Orphanet:794)
Schilbach-Rott syndrome (Orphanet:2353)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Split hand - urinary anomalies - spina bifida (Orphanet:2437)
Stapes ankylosis with broad thumbs and toes (Orphanet:140917)
Symphalangism with multiple anomalies of hands and feet (Orphanet:3246)
Syndactyly - telecanthus - anogenital and renal malformations (Orphanet:140952)
Syndactyly type 1 (Orphanet:93402)
Syndactyly type 2 (Orphanet:93403)
Syndactyly type 4 (Orphanet:93405)
Syndactyly type 5 (Orphanet:93406)
Syndrome with brachydactyly (Orphanet:69028)
Synpolydactyly type 2 (Orphanet:295197)
Timothy syndrome (Orphanet:65283)
Toriello-Carey syndrome (Orphanet:3338)
Townes-Brocks syndrome (Orphanet:857)
Triphalangeal thumb - polysyndactyly syndrome (Orphanet:2950)
Trisomy 1q (Orphanet:261344)
Ulnar/fibula ray defect - brachydactyly (Orphanet:52056)
Urban-Rogers-Meyer syndrome (Orphanet:3409)
Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay (Orphanet:73246)
Yunis-Varon syndrome (Orphanet:3472)
Zlotogora-Ogur syndrome (Orphanet:3253)