Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Excision of supernumerary finger (procedure) |
Procedure site - Direct (attribute) |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Reamputation of finger (procedure) |
Procedure site - Direct (attribute) |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Nonvenomous insect bite of finger (disorder) |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
1 |
Superficial foreign body in finger |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
1 |
Excision of ganglion cyst of finger (procedure) |
Procedure site - Direct (attribute) |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Revision of amputation stump of finger (procedure) |
Procedure site |
False |
Finger structure |
Inferred relationship |
Some |
1 |
Primary malignant neoplasm of blood vessel of finger |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Neoplasm of blood vessel of finger |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
2 |
Camptodactyly-little finger (disorder) |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
3 |
Central polydactyly of fingers |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Radial polydactyly Wassel 1 |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Macrodactyly of fingers- fatty nerve tumor |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Macrodactyly of fingers - simple |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Radial polydactyly Wassel 3 |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Ulnar polydactyly of fingers |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Congenital anomaly of finger (disorder) |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Radial polydactyly |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Radial polydactyly Wassel 5 |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Congenital hypoplasia of finger (disorder) |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Radial polydactyly Wassel 4 |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Radial polydactyly Wassel 7 |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Proximal interphalangeal joint symphalangism |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Radial polydactyly Wassel 2 |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Distal interphalangeal joint symphalangism |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Radial polydactyly Wassel 6 |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Polydactyly of fingers |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Triphalangeal thumb |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Macrodactylia of fingers |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Complete aphalangia of upper limb |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Partial aphalangia of upper limb |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Camptodactyly |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
3 |
Congenital absence of finger |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Acrosyndactyly of the fingers |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
5 |
Congenital anomaly of finger (disorder) |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Camptodactyly |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Syndactyly of fingers |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Excision of constriction ring of finger with Z plasty (procedure) |
Procedure site - Direct (attribute) |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Syndactyly of fingers |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
3 |
Excision of hemangioma of finger |
Procedure site - Indirect (attribute) |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Constriction ring of upper limb with acrosyndactyly and amputation |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
Tsuge operation on finger for macrodactyly repair |
Procedure site - Direct (attribute) |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Polydactyly of fingers |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
Radial polydactyly Wassel 1 |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
Radial polydactyly Wassel 2 |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
Radial polydactyly Wassel 3 |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
Radial polydactyly Wassel 4 |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
Radial polydactyly Wassel 5 |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
Radial polydactyly Wassel 6 |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
Radial polydactyly Wassel 7 |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
Central polydactyly of fingers |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
Ulnar polydactyly of fingers |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
Radial polydactyly |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
Camptodactyly-little finger (disorder) |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Acrosyndactyly of the fingers |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Acute lymphangitis of finger |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
3 |
Repair of finger (procedure) |
Procedure site - Direct (attribute) |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Syndactyly of fingers type 8 (disorder) |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
1 |
A rare non-syndromic syndactyly characterized by complete and bilateral syndactyly between the 4th and 5th fingers. In most cases, it is a soft tissue syndactyly, but occasionally the distal phalanges may be fused. The middle phalanx of the fifth finger is usually hypoplastic, and the feet are not affected. |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
1 |
A rare syndrome characterized by mesomelic shortening and bowing of the limbs, camptodactyly, skin dimpling and cleft palate with retrognathia and mandibular hypoplasia. It has been described in a brother and sister born to consanguineous parents. Transmission is autosomal recessive. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
9 |
A rare congenital limb malformation characterized by duplication of the fifth digit in a hand or foot, with an extra, well-formed, functional digit at the metacarpophalangeal/metatarsophalangeal or carpometacarpal/tarsometatarsal joint. The malformation can be an isolated finding or be associated with a large number of other anomalies. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
A rare congenital limb malformation characterized by duplication of the fifth digit in a hand or foot, with an extra, well-formed, functional digit at the metacarpophalangeal/metatarsophalangeal or carpometacarpal/tarsometatarsal joint. The malformation can be an isolated finding or be associated with a large number of other anomalies. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
5 |
A rare congenital limb malformation characterized by duplication of the fifth digit in a hand or foot, the sixth digit being rudimentary, poorly developed, and non-functional, frequently consisting of additional soft tissue on a pedicle. The anomaly can be unilateral or bilateral. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
A rare congenital limb malformation characterized by duplication of the fifth digit in a hand or foot, the sixth digit being rudimentary, poorly developed, and non-functional, frequently consisting of additional soft tissue on a pedicle. The anomaly can be unilateral or bilateral. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
5 |
A rare multiple congenital anomalies syndrome characterized by the association of camptodactyly, multiple eye defects (fibrosis of the medial rectus muscle, severe myopia, ptosis and exophthalmos), scoliosis, flexion contractures and facial anomalies (arched eyebrows, facial asymmetry with an abnormal skull shape, a prominent nose, small mouth, low-set and dysplastic ears, and a low nuchal hairline). |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
7 |
Structure of finger of left hand (body structure) |
Is a |
True |
Finger structure |
Inferred relationship |
Some |
|
Structure of finger of right hand (body structure) |
Is a |
True |
Finger structure |
Inferred relationship |
Some |
|
Toe to finger transfer, second stage |
Procedure site - Direct (attribute) |
True |
Finger structure |
Inferred relationship |
Some |
4 |
Tel Hashomer camptodactyly syndrome is a rare syndrome characterized by camptodactyly, muscle hypoplasia and weakness, skeletal anomalies, facial dysmorphism and abnormal dermatoglyphics. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
An extremely rare chondrodysplastic malformation syndrome characterised by the combination of arachnodactyly, becoming evident at around the age of 10, camptodactyly, and scoliosis. Additional reported manifestations include a mild intellectual disability and a mild facial dysmorphism including a broad nose and flaring nostrils. There have been no further descriptions in the literature since 1972. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
8 |
Camptodactyly-tall stature-scoliosis-hearing loss syndrome is characterized by camptodactyly, tall stature, scoliosis, and hearing loss (CATSHL). It has been described in around 30 individuals from seven generations of the same family. The syndrome is caused by a missense mutation in the FGFR3 gene, leading to a partial loss of function of the encoded protein, which is a negative regulator of bone growth. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
6 |
Camptodactyly syndrome, Guadalajara type 2 is an extremely rare multiple congenital anomaly syndrome characterized by distinctive intrauterine growth retardation, skeletal dysplasia with multiple malformations including camptodactyly of all fingers, bilateral hallux valgus, short second, fourth and fifth toes, hypoplastic patella, microcephaly, low-set ears, short neck, cuboid-shaped vertebral bodies, pectus excavatum, hip dislocation, and hypoplastic pubic region and genitalia. Camptodactyly syndrome, Guadalajara type 2 has been described in two sisters and is most likely transmitted in an autosomal recessive manner. There have been no further descriptions in the literature since 1985. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
5 |
Camptodactyly syndrome, Guadalajara type 1 is a rare syndrome consisting of growth retardation, facial dysmorphism, camptodactyly and skeletal anomalies. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
Guttmacher syndrome is an extremely rare syndrome characterized by hypoplastic thumbs and halluces, 5th finger clinobrachydactyly, postaxial polydactyly of the hands, short or uniphalangeal 2nd toes with absent nails and hypospadias. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
6 |
A rare congenital limb malformation characterized by duplication of the fifth digit in a hand or foot, with an extra, well-formed, functional digit at the metacarpophalangeal/metatarsophalangeal or carpometacarpal/tarsometatarsal joint. The malformation can be an isolated finding or be associated with a large number of other anomalies. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
1 |
A rare congenital limb malformation characterized by duplication of the fifth digit in a hand or foot, the sixth digit being rudimentary, poorly developed, and non-functional, frequently consisting of additional soft tissue on a pedicle. The anomaly can be unilateral or bilateral. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
1 |
Crisponi syndrome (CS) is a severe disorder characterized by muscular contractions at birth, intermittent hyperthermia, facial abnormalities and camptodactyly. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
5 |
Structure of soft tissue of finger (body structure) |
Is a |
True |
Finger structure |
Inferred relationship |
Some |
|
Problem of finger (finding) |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Eyebrow duplication-syndactyly syndrome is characterized by partial duplication of the eyebrows and syndactyly of the fingers and toes. It has been described in three patients (a brother and sister and an isolated case). Skin hyperelasticity, hypertrichosis and long eyelashes, and abnormal periorbital wrinkling were also reported in some of the patients. Transmission is autosomal recessive. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
4 |
Open bite of finger (disorder) |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Laceration of finger with foreign body (disorder) |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
2 |
Laceration of finger with foreign body (disorder) |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
3 |
Puncture wound of finger with foreign body (disorder) |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
2 |
Puncture wound of finger with foreign body (disorder) |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
3 |
Laceration of finger without foreign body (disorder) |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Puncture wound of finger without foreign body (disorder) |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Laceration of blood vessel of finger (disorder) |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Repair of macrodactyly of finger |
Procedure site - Direct (attribute) |
False |
Finger structure |
Inferred relationship |
Some |
2 |
Viral wart on finger (disorder) |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Structure of nail unit of finger (body structure) |
Is a |
False |
Finger structure |
Inferred relationship |
Some |
|
A rare multiple congenital anomalies syndrome characterized by the association of camptodactyly, multiple eye defects (fibrosis of the medial rectus muscle, severe myopia, ptosis and exophthalmos), scoliosis, flexion contractures and facial anomalies (arched eyebrows, facial asymmetry with an abnormal skull shape, a prominent nose, small mouth, low-set and dysplastic ears, and a low nuchal hairline). |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
3 |
A rare syndrome characterized by mesomelic shortening and bowing of the limbs, camptodactyly, skin dimpling and cleft palate with retrognathia and mandibular hypoplasia. It has been described in a brother and sister born to consanguineous parents. Transmission is autosomal recessive. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
3 |
Constriction ring of upper limb with acrosyndactyly and amputation |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Camptodactyly syndrome, Guadalajara type 2 is an extremely rare multiple congenital anomaly syndrome characterized by distinctive intrauterine growth retardation, skeletal dysplasia with multiple malformations including camptodactyly of all fingers, bilateral hallux valgus, short second, fourth and fifth toes, hypoplastic patella, microcephaly, low-set ears, short neck, cuboid-shaped vertebral bodies, pectus excavatum, hip dislocation, and hypoplastic pubic region and genitalia. Camptodactyly syndrome, Guadalajara type 2 has been described in two sisters and is most likely transmitted in an autosomal recessive manner. There have been no further descriptions in the literature since 1985. |
Finding site |
False |
Finger structure |
Inferred relationship |
Some |
3 |
Guttmacher syndrome is an extremely rare syndrome characterized by hypoplastic thumbs and halluces, 5th finger clinobrachydactyly, postaxial polydactyly of the hands, short or uniphalangeal 2nd toes with absent nails and hypospadias. |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Tel Hashomer camptodactyly syndrome is a rare syndrome characterized by camptodactyly, muscle hypoplasia and weakness, skeletal anomalies, facial dysmorphism and abnormal dermatoglyphics. |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
2 |
Camptodactyly-tall stature-scoliosis-hearing loss syndrome is characterized by camptodactyly, tall stature, scoliosis, and hearing loss (CATSHL). It has been described in around 30 individuals from seven generations of the same family. The syndrome is caused by a missense mutation in the FGFR3 gene, leading to a partial loss of function of the encoded protein, which is a negative regulator of bone growth. |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
2 |
Eyebrow duplication-syndactyly syndrome is characterized by partial duplication of the eyebrows and syndactyly of the fingers and toes. It has been described in three patients (a brother and sister and an isolated case). Skin hyperelasticity, hypertrichosis and long eyelashes, and abnormal periorbital wrinkling were also reported in some of the patients. Transmission is autosomal recessive. |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
2 |
Crisponi syndrome (CS) is a severe disorder characterized by muscular contractions at birth, intermittent hyperthermia, facial abnormalities and camptodactyly. |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
1 |
Camptodactyly syndrome, Guadalajara type 1 is a rare syndrome consisting of growth retardation, facial dysmorphism, camptodactyly and skeletal anomalies. |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
3 |
An extremely rare chondrodysplastic malformation syndrome characterised by the combination of arachnodactyly, becoming evident at around the age of 10, camptodactyly, and scoliosis. Additional reported manifestations include a mild intellectual disability and a mild facial dysmorphism including a broad nose and flaring nostrils. There have been no further descriptions in the literature since 1972. |
Finding site |
True |
Finger structure |
Inferred relationship |
Some |
2 |