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7569003: Finger structure (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
13486012 Finger en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
503086016 Finger structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
816328011 Finger structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
891391000172112 structure du doigt de la main, sauf le pouce fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
906051000172117 doigt fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1003951000172119 doigt de la main, sauf le pouce fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6990711000241110 structure d'un doigt de la main, sauf le pouce fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1275 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Finger structure Is a Digit of hand structure true Inferred relationship Some
Finger structure partie de Entire hand false Additional relationship Some
Finger structure Laterality Side (qualifier value) true Inferred relationship Some

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

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Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

Anatomy structure and entire association reference set (foundation metadata concept)

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