Syndactyly

Symptom Information:

Symptom ID: HPO:0001159
Synonyms:
Syndactyly [OMIM:Syndactyly]
syndactyly [OMIM: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. [OMIM:Syndactyly.]
Quality:
Cross references:
OMIM: "Syndactyly" [OMIM:Syndactyly]
OMIM: "syndactyly" [OMIM: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." [OMIM:Syndactyly.]
UMLS:C0039075 "Syndactyly" [HPO:0001159]
Is a (Direct Parents):
HPO         Abnormality of digit
HPO         Cutaneous 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)
                      Syndactyly(HPO:0001159)
MedDRA:
Database Frequency: 140 / 7739
Resource:

All diseases associated with this symptom:

3C syndrome (Orphanet:7)
8q21.11 microdeletion syndrome (Orphanet:284160)
AARSKOG-SCOTT SYNDROME (OMIM:305400)
ADAMS-OLIVER SYNDROME 1 (OMIM:100300)
ADAMS-OLIVER SYNDROME 5 (OMIM:616028)
ADULT syndrome (Orphanet:978)
AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM (OMIM:104350)
ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib (OMIM:615631)
Aarskog-Scott syndrome (Orphanet:915)
Acro-renal-mandibular syndrome (Orphanet:958)
Acro-renal-ocular syndrome (Orphanet:959)
Acromelic frontonasal dysplasia (Orphanet:1827)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 4 (OMIM:615982)
Bardet-Biedl syndrome 6 (OMIM:605231)
Bardet-Biedl syndrome 7 (OMIM:615984)
Bardet-Biedl syndrome 9 (OMIM:615986)
Bartsocas-Papas syndrome (Orphanet:1234)
Bloom syndrome (Orphanet:125)
Bohring-Opitz syndrome (Orphanet:97297)
Brachydactyly type A2 (Orphanet:93396)
Brachydactyly type B (Orphanet:93383)
C syndrome (Orphanet:1308)
CARPENTER SYNDROME 1 (OMIM:201000)
CORNELIA DE LANGE SYNDROME 4 (OMIM:614701)
Camptobrachydactyly (Orphanet:1319)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Cenani-Lenz syndrome (Orphanet:3258)
Charcot-Marie-Tooth disease type 4B3 (Orphanet:363981)
Congenital dyserythropoietic anemia type I (Orphanet:98869)
Constriction rings syndrome (Orphanet:295000)
Cranioectodermal dysplasia 2 (OMIM:613610)
Cranioectodermal dysplasia 3 (OMIM:614099)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
Craniofrontonasal dysplasia (Orphanet:1520)
Craniosynostosis and dental anomalies (Orphanet:284149)
Curry-Jones syndrome (Orphanet:1553)
Diaphragmatic defect - limb deficiency - skull defect (Orphanet:2141)
Distal monosomy 10q (Orphanet:96148)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEM syndrome (Orphanet:1897)
Endocrine-cerebro-osteodysplasia syndrome (Orphanet:199332)
FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME (OMIM:246570)
Faciocardiorenal syndrome (Orphanet:1973)
Fibulo-ulnar hypoplasia - renal anomalies (Orphanet:2256)
Focal dermal hypoplasia (Orphanet:2092)
Fraser syndrome (Orphanet:2052)
Fuhrmann syndrome (Orphanet:2854)
Goodman syndrome (Orphanet:65798)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
Hallux varus - preaxial polysyndactyly (Orphanet:2110)
Hartsfield-Bixler-Demyer syndrome (Orphanet:2117)
Heart-hand syndrome, Slovenian type (Orphanet:168796)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Hypoplastic tibiae - postaxial polydactyly (Orphanet:3332)
Ito hypomelanosis (Orphanet:435)
Jawad syndrome (Orphanet:313795)
Joubert syndrome 17 (OMIM:614615)
Joubert syndrome 20 (OMIM:614970)
Joubert syndrome 22 (OMIM:615665)
KBG syndrome (Orphanet:2332)
Klippel-Trénaunay syndrome (Orphanet:90308)
LOEYS-DIETZ SYNDROME 2 (OMIM:610168)
Langer-Giedion syndrome (Orphanet:502)
Lathosterolosis (Orphanet:46059)
Laurin-Sandrow syndrome (Orphanet:2378)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Limb-mammary syndrome (Orphanet:69085)
MICROPHTHALMIA, SYNDROMIC 1 (OMIM:309800)
McKusick-Kaufman syndrome (Orphanet:2473)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 1 (OMIM:249000)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Microduplication Xp11.22-p11.23 syndrome (Orphanet:217377)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Microphthalmia with limb anomalies (Orphanet:1106)
Moebius syndrome (Orphanet:570)
Monosomy 18q (Orphanet:1600)
Monosomy 5p (Orphanet:281)
Nager syndrome (Orphanet:245)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
OROFACIODIGITAL SYNDROME VI (OMIM:277170)
Okihiro syndrome (Orphanet:93293)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Orofaciodigital syndrome type 8 (Orphanet:2755)
Orofaciodigital syndrome type 9 (Orphanet:141007)
Otopalatodigital syndrome type 2 (Orphanet:90652)
Pallister-Hall syndrome (Orphanet:672)
Pelviscapular dysplasia (Orphanet:93333)
Peters-plus syndrome (Orphanet:709)
Poland syndrome (Orphanet:2911)
Polysyndactyly - cardiac malformation (Orphanet:2934)
Postaxial acrofacial dysostosis (Orphanet:246)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Postaxial polydactyly type A (Orphanet:93334)
Prader-Willi syndrome (Orphanet:739)
Pseudoaminopterin syndrome (Orphanet:221120)
RAPP-HODGKIN SYNDROME (OMIM:129400)
ROBERTS SYNDROME (OMIM:268300)
Radio-ulnar synostosis - amegakaryocytic thrombocytopenia (Orphanet:71289)
Roberts syndrome (Orphanet:3103)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
SANTOS SYNDROME (OMIM:613005)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
SPINAL MUSCULAR ATROPHY WITH MENTAL RETARDATION (OMIM:271109)
SPLIT-HAND/FOOT MALFORMATION 4 (OMIM:605289)
Saethre-Chotzen syndrome (Orphanet:794)
Sakati-Nyhan syndrome (Orphanet:3128)
Schilbach-Rott syndrome (Orphanet:2353)
Short-rib thoracic dysplasia 7 with or without polydactyly (OMIM:614091)
Short-rib thoracic dysplasia 8 with or without polydactyly (OMIM:615503)
Silver-Russell syndrome (Orphanet:813)
Split hand-split foot malformation (Orphanet:2440)
Stapes ankylosis with broad thumbs and toes (Orphanet:140917)
Summitt syndrome (Orphanet:3210)
Symphalangism with multiple anomalies of hands and feet (Orphanet:3246)
Syndactyly - camptodactyly and clinodactyly of fifth fingers - bifid toes (Orphanet:357332)
Syndactyly type 3 (Orphanet:93404)
Synpolydactyly type 2 (Orphanet:295197)
TUKEL SYNDROME (OMIM:609428)
Temtamy preaxial brachydactyly syndrome (Orphanet:363417)
Timothy syndrome (Orphanet:65283)
Triphalangeal thumb - polysyndactyly syndrome (Orphanet:2950)
Ulnar/fibula ray defect - brachydactyly (Orphanet:52056)
VACTERL/VATER association (Orphanet:887)
Verloove Vanhorick-Brubakk syndrome (Orphanet:3429)
Waardenburg syndrome type 3 (Orphanet:896)
Yunis-Varon syndrome (Orphanet:3472)