Finger syndactyly

Symptom Information:

Symptom ID: HPO:0006101
Partial syndactyly [HPO:0006101]
Finger syndactyly [OMIM:Finger syndactyly]
Partial syndactyly [OMIM:Partial syndactyly]
Cross references:
OMIM: "Finger syndactyly" [OMIM:Finger syndactyly]
OMIM: "Partial syndactyly" [OMIM:Partial syndactyly]
Is a (Direct Parents):
HPO         Syndactyly
Is a (Whole tree): HPO:
    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)
                         Finger syndactyly(HPO:0006101)
Database Frequency: 198 / 7739

All diseases associated with this symptom:

14q22q23 microdeletion syndrome (Orphanet:264200)
15q11q13 microduplication syndrome (Orphanet:238446)
15q24 microdeletion syndrome (Orphanet:94065)
17q12 microduplication syndrome (Orphanet:261272)
19p13.12 microdeletion syndrome (Orphanet:254346)
19q13.11 microdeletion syndrome (Orphanet:217346)
2q31.1 microdeletion syndrome (Orphanet:251014)
2q37 microdeletion syndrome (Orphanet:1001)
3C syndrome (Orphanet:7)
6p22 microdeletion syndrome (Orphanet:251046)
8q21.11 microdeletion syndrome (Orphanet:284160)
8q22.1 microdeletion syndrome (Orphanet:178303)
ADULT syndrome (Orphanet:978)
Aarskog-Scott syndrome (Orphanet:915)
Ackerman syndrome (Orphanet:2561)
Acro-cardio-facial syndrome (Orphanet:2008)
Acro-oto-ocular syndrome (Orphanet:2980)
Acro-pectoral syndrome (Orphanet:85203)
Acro-pectoro-renal dysplasia (Orphanet:956)
Acro-renal-mandibular syndrome (Orphanet:958)
Acro-renal-ocular syndrome (Orphanet:959)
Acrocallosal syndrome (Orphanet:36)
Acrofacial dysostosis, Catania type (Orphanet:1786)
Acrofacial dysostosis, Palagonia type (Orphanet:1787)
Acrofacial dysostosis, Rodriguez type (Orphanet:1788)
Acropectorovertebral dysplasia (Orphanet:957)
Adams-Oliver syndrome (Orphanet:974)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Aminopterin/methotrexate embryofetopathy (Orphanet:1908)
Amniotic bands (Orphanet:1034)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Apert syndrome (Orphanet:87)
Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis (Orphanet:1112)
Autosomal dominant Larsen syndrome (Orphanet:503)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant popliteal pterygium syndrome (Orphanet:1300)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Autosomal recessive spondylocostal dysostosis (Orphanet:2311)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 4 (OMIM:615982)
Bartsocas-Papas syndrome (Orphanet:1234)
Blepharo-cheilo-odontic syndrome (Orphanet:1997)
Blepharonasofacial malformation syndrome (Orphanet:1252)
Bloom syndrome (Orphanet:125)
Boomerang dysplasia (Orphanet:1263)
Brachydactyly type B (Orphanet:93383)
Brachydactyly type B2 (Orphanet:140908)
Camptobrachydactyly (Orphanet:1319)
Camptodactyly - joint contractures - facial skeletal defects (Orphanet:1323)
Cenani-Lenz syndrome (Orphanet:3258)
Charlie M syndrome (Orphanet:1406)
Choroidal atrophy - alopecia (Orphanet:1433)
Cohen syndrome (Orphanet:193)
Crane-Heise syndrome (Orphanet:1512)
Cranioectodermal dysplasia (Orphanet:1515)
Craniofrontonasal dysplasia (Orphanet:1520)
Craniomicromelic syndrome (Orphanet:1524)
Craniosynostosis, Herrmann-Opitz type (Orphanet:2145)
Craniosynostosis, Philadelphia type (Orphanet:1527)
Crossed polysyndactyly (Orphanet:2935)
Curry-Jones syndrome (Orphanet:1553)
Cutis marmorata telangiectatica congenita (Orphanet:1556)
Deafness - genital anomalies - metacarpal and metatarsal synostosis (Orphanet:3224)
Diaphragmatic defect - limb deficiency - skull defect (Orphanet:2141)
Dystrophic epidermolysis bullosa (Orphanet:303)
EEC syndrome (Orphanet:1896)
EEM syndrome (Orphanet:1897)
Ectodermal dysplasia syndrome (Orphanet:79373)
Ectrodactyly - polydactyly (Orphanet:1892)
Embryonary disorganization syndrome (Orphanet:1664)
Epiphyseal dysplasia - hearing loss - dysmorphism (Orphanet:1825)
Eyebrow duplication - syndactyly (Orphanet:3172)
FACES syndrome (Orphanet:1969)
Fanconi anemia (Orphanet:84)
Femur-fibula-ulna complex (Orphanet:2019)
Fibulo-ulnar hypoplasia - renal anomalies (Orphanet:2256)
Filippi syndrome (Orphanet:3255)
Fine-Lubinsky syndrome (Orphanet:1272)
Focal dermal hypoplasia (Orphanet:2092)
Fraser syndrome (Orphanet:2052)
Fuhrmann syndrome (Orphanet:2854)
Goldberg-Shprintzen megacolon syndrome (Orphanet:66629)
Gordon syndrome (Orphanet:376)
Gorlin syndrome (Orphanet:377)
Grange syndrome (Orphanet:79094)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
Heart defect - tongue hamartoma - polysyndactyly (Orphanet:1338)
Hennekam syndrome (Orphanet:2136)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hereditary spastic paraplegia (Orphanet:685)
Hidrotic ectodermal dysplasia (Orphanet:189)
Holt-Oram syndrome (Orphanet:392)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Hypertelorism, Teebi type (Orphanet:1519)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Hypoglossia - hypodactyly (Orphanet:989)
Hypoplastic tibiae - postaxial polydactyly (Orphanet:3332)
Incontinentia pigmenti (Orphanet:464)
Intellectual deficit - spasticity - ectrodactyly (Orphanet:1891)
Isolated cloverleaf skull syndrome (Orphanet:2343)
Jackson-Weiss syndrome (Orphanet:1540)
Jacobsen syndrome (Orphanet:2308)
Junctional epidermolysis bullosa (Orphanet:305)
Junctional epidermolysis bullosa, Herlitz type (Orphanet:79404)
KBG syndrome (Orphanet:2332)
Kindler syndrome (Orphanet:2908)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Laurence-Moon syndrome (Orphanet:2377)
Laurin-Sandrow syndrome (Orphanet:2378)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Limb transversal defect - cardiac anomaly (Orphanet:2492)
Mal de Meleda (Orphanet:87503)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
McKusick-Kaufman syndrome (Orphanet:2473)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Mesoaxial synostotic syndactyly with phalangeal reduction (Orphanet:157801)
Mesomelic dwarfism, Nievergelt type (Orphanet:2633)
Microcephaly - intellectual deficit - phalangeal and neurological anomalies (Orphanet:137658)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Microphthalmia with limb anomalies (Orphanet:1106)
Microphthalmia, Lenz type (Orphanet:568)
Moebius syndrome (Orphanet:570)
Monosomy 13q14 (Orphanet:1587)
Monosomy 5p (Orphanet:281)
Mowat-Wilson syndrome (Orphanet:2152)
Multiple epiphyseal dysplasia, Al-Gazali type (Orphanet:166024)
Neu-Laxova syndrome (Orphanet:2671)
Nevus comedonicus syndrome (Orphanet:64754)
Oculocerebrocutaneous syndrome (Orphanet:1647)
Oculodentodigital dysplasia (Orphanet:2710)
Odontotrichomelic syndrome (Orphanet:2723)
Okamoto syndrome (Orphanet:2729)
Oliver syndrome (Orphanet:2920)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Orofaciodigital syndrome type 5 (Orphanet:2919)
Orofaciodigital syndrome type 8 (Orphanet:2755)
Otopalatodigital syndrome (Orphanet:669)
Pallister-Hall syndrome (Orphanet:672)
Paraplegia - brachydactyly - cone-shaped epiphysis (Orphanet:2823)
Pfeiffer syndrome (Orphanet:710)
Pfeiffer syndrome type 1 (Orphanet:93258)
Pfeiffer syndrome type 2 (Orphanet:93259)
Pfeiffer syndrome type 3 (Orphanet:93260)
Poland syndrome (Orphanet:2911)
Polysyndactyly - cardiac malformation (Orphanet:2934)
Postaxial acrofacial dysostosis (Orphanet:246)
Proteus syndrome (Orphanet:744)
Proximal symphalangism (Orphanet:3250)
Radio-ulnar synostosis - amegakaryocytic thrombocytopenia (Orphanet:71289)
Recessive aplasia cutis congenita of limbs (Orphanet:1115)
Recessive dystrophic epidermolysis bullosa-generalized other (Orphanet:89842)
Roberts syndrome (Orphanet:3103)
Rubinstein-Taybi syndrome (Orphanet:783)
Saethre-Chotzen syndrome (Orphanet:794)
Schilbach-Rott syndrome (Orphanet:2353)
Sclerosteosis (Orphanet:3152)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Short rib-polydactyly syndrome (Orphanet:1505)
Short stature - craniofacial anomalies - genital hypoplasia (Orphanet:2994)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Split hand - urinary anomalies - spina bifida (Orphanet:2437)
Split hand-split foot malformation (Orphanet:2440)
Summitt syndrome (Orphanet:3210)
Symphalangism with multiple anomalies of hands and feet (Orphanet:3246)
Syndactyly type 1 (Orphanet:93402)
Syndactyly type 2 (Orphanet:93403)
Syndactyly type 3 (Orphanet:93404)
Syndactyly type 4 (Orphanet:93405)
Syndactyly type 5 (Orphanet:93406)
Syndrome with brachydactyly (Orphanet:69028)
Synostosis - microcephaly - scoliosis (Orphanet:3268)
Synpolydactyly type 1 (Orphanet:295195)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Thrombocytopenia - absent radius (Orphanet:3320)
Thumb deformity - alopecia - pigmentation anomaly (Orphanet:2251)
Tibial aplasia - ectrodactyly (Orphanet:3329)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Tricho-odonto-onychodysplasia - dominant syndactyly (Orphanet:3357)
Triphalangeal thumb - polysyndactyly syndrome (Orphanet:2950)
Triploidy (Orphanet:3376)
Trisomy 20p (Orphanet:261318)
VACTERL/VATER association (Orphanet:887)
Van Regemorter-Pierquin-Vamos syndrome (Orphanet:3419)
Verloove Vanhorick-Brubakk syndrome (Orphanet:3429)
Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay (Orphanet:73246)
WT limb-blood syndrome (Orphanet:3466)
Waardenburg syndrome type 3 (Orphanet:896)
Weaver syndrome (Orphanet:3447)
White forelock with malformations (Orphanet:2475)
Zlotogora-Ogur syndrome (Orphanet:3253)