Finger symphalangism

Symptom Information:

Symptom ID: HPO:0009700
Synonyms:
Symphalangism of the hand [HPO:0009700]
Fingers symphalangy [Orphanet:20460]
Syndactyly of fingers with fusion of bones (disorder) [Orphanet:20460]
Syndactyly of fingers with fusion of bones [Orphanet:20460]
Symphalangy of fingers [Orphanet:20460]
Syndactyly of fingers with fusion of bone [Orphanet:20460]
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]
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. [OMIM:Syndactyly.]
Webbed fingers [OMIM:Webbed fingers]
Quality:
Cross references:
Orphanet:20460 "Symphalangy of fingers" [Orphanet:20460]
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." [OMIM:Syndactyly.]
OMIM: "Webbed fingers" [OMIM:Webbed fingers]
UMLS:C0158736 "Syndactyly of fingers with fusion of bones" [Orphanet:20460]
Is a (Direct Parents):
HPO         Synostosis involving bones of the hand
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
Orphanet Abnormality of the hand
HPO         Synostosis involving digits
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 joint morphology(HPO:0001367)
                Abnormality of joint mobility(HPO:0011729)
                   Synostosis of joints(HPO:0100240)
                      Synostosis involving bones of the upper limbs(HPO:0100238)
                         Synostosis involving bones of the hand(HPO:0004278)
                            Finger symphalangism(HPO:0009700)
                      Synostosis involving digits(HPO:0100262)
                         Finger symphalangism(HPO:0009700)
                Abnormality of upper limb joint(HPO:0009810)
                   Synostosis involving bones of the upper limbs(HPO:0100238)
                      Synostosis involving bones of the hand(HPO:0004278)
                         Finger symphalangism(HPO:0009700)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Synostosis involving bones of the hand(HPO:0004278)
                            Finger symphalangism(HPO:0009700)
                      Abnormality of upper limb joint(HPO:0009810)
                         Synostosis involving bones of the upper limbs(HPO:0100238)
                            Synostosis involving bones of the hand(HPO:0004278)
                               Finger symphalangism(HPO:0009700)
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)
          Finger symphalangism(HPO:0009700)
Database Frequency: 55 / 7739
Resource:

All diseases associated with this symptom:

Aphalangy - syndactyly - microcephaly (Orphanet:1113)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Brachydactyly type A1 (Orphanet:93388)
Brachydactyly type A2 (Orphanet:93396)
Brachydactyly type A4 (Orphanet:93394)
Brachydactyly type B (Orphanet:93383)
Brachydactyly type B2 (Orphanet:140908)
Brachydactyly type C (Orphanet:93384)
Brachydactyly-syndactyly, Zhao type (Orphanet:93409)
Brachymorphism - onychodysplasia - dysphalangism (Orphanet:1292)
CORNELIA DE LANGE SYNDROME 4 (OMIM:614701)
CREE MENTAL RETARDATION SYNDROME (OMIM:606851)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Caudal appendage - deafness (Orphanet:1123)
Char syndrome (Orphanet:46627)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
Craniofrontonasal dysplasia (Orphanet:1520)
Craniosynostosis and dental anomalies (Orphanet:284149)
Curry-Jones syndrome (Orphanet:1553)
Deafness - onychodystrophy (Orphanet:3231)
Diastrophic dwarfism (Orphanet:628)
Distal monosomy 7q36 (Orphanet:1636)
Distal symphalangism (Orphanet:3248)
Ectrodactyly - polydactyly (Orphanet:1892)
Faciocardiorenal syndrome (Orphanet:1973)
Focal dermal hypoplasia (Orphanet:2092)
Fuhrmann syndrome (Orphanet:2854)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Jackson-Weiss syndrome (Orphanet:1540)
Joubert syndrome 17 (OMIM:614615)
Joubert syndrome 20 (OMIM:614970)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
MULTIPLE SYNOSTOSES SYNDROME 2 (OMIM:610017)
Mesoaxial synostotic syndactyly with phalangeal reduction (Orphanet:157801)
Microphthalmia - microtia - fetal akinesia (Orphanet:2547)
Mononen-Karnes-Senac syndrome (Orphanet:2565)
Multiple synostoses syndrome (Orphanet:3237)
Oliver syndrome (Orphanet:2920)
Ophthalmomandibulomelic dysplasia (Orphanet:2741)
Pelviscapular dysplasia (Orphanet:93333)
Pfeiffer syndrome (Orphanet:710)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Proximal symphalangism (Orphanet:3250)
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)
Syndactyly type 1 (Orphanet:93402)
Syndactyly type 2 (Orphanet:93403)
Syndrome with brachydactyly (Orphanet:69028)
Synpolydactyly type 2 (Orphanet:295197)
Timothy syndrome (Orphanet:65283)
Trismus - pseudocamptodactyly (Orphanet:3377)
Ulnar/fibula ray defect - brachydactyly (Orphanet:52056)