361367007: Entire digit (body structure)

SNOMED CT Concept\Body structure\Anatomical or acquired body structure (body structure)\Anatomical structure\Body region structure\...

\Structure of half of body lateral to midsagittal plane\Limb structure\Extremity part\Digit structure\Entire digit

\Body part structure\Limb structure\Extremity part\Digit structure\Entire digit

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Entire digit	Is a	Entire body part	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Entire digit	Is a	Digit structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Entire digit	partie de	Entire limb	false	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
Entire digit	Laterality	Side	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Structure of middle phalanx of foot (body structure)	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
Structure of proximal phalanx of foot (body structure)	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
Bone part of distal phalanx of finger	partie de	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)
Entire articular surface, phalanges, of fifth metacarpal bone	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
Structure of articular surface, phalanges, of fifth metacarpal bone	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
Entire third phalanx of digit III of equine limb	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
Pastern bones of hindlimb	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
Pastern bones of forelimb	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
P3 of ruminant digit IV	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
P3 of ruminant digit III	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
P3 of Digit III of equine limb (body structure)	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
P3 of Digit III of equine hindlimb	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
P3 of Digit III of equine forelimb	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
P2 of ruminant digit IV	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
P2 of ruminant digit III	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
P2 of Digit III of equine hindlimb	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
P2 of Digit III of equine forelimb	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
P2 of digit III of equine limb	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
P1 of ruminant digit III	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
P1 of Digit III of equine limb	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
P1 of Digit III of equine hindlimb	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
P1 of Digit III of equine forelimb	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
Interphalangeal joint structure (body structure)	partie de	False	Entire digit	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)
Cleft hand with syndactyly (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Cleft hand with polydactyly	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Cleft hand - central (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital cleft hand	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ectrodactyly (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Split foot	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Cleft hand - first cleft	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ectrodactyly-ectodermal dysplasia-clefting syndrome	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Sarcoid dactylitis	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hand-foot syndrome in sickle cell anemia (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Tuberculous dactylitis	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Dactylitis	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Blistering distal dactylitis	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Psoriatic dactylitis	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Tibial aplasia-ectrodactyly syndrome is a rare condition characterized by congenital ectrodactylous limb malformations associated with tibial aplasia or hypoplasia.	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
The MMEP syndrome is a congenital syndromic form of split-hand/foot malformation. It is characterized by microcephaly, microphthalmia, ectrodactyly of the lower limbs and prognathism. Intellectual deficit has been reported. MMEP syndrome is considered to be a very rare condition, although the exact prevalence remains unknown. The etiology is not completely understood. Disruption of the sorting nexin 3 gene (SNX3; 6q21) has been shown to play a causative role in MMEP, although this was not confirmed in recent studies.	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	7
A rare congenital limb malformation characterized by bifid femur, absent or hypoplastic tibia and ulna with limb shortening, oligodactyly, and ectrodactyly.	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Cooks syndrome (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Weill-Marchesani syndrome	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Brachymegalodactyly	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Brachydactyly	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Brachydactyly syndrome type E	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Microdactyly	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
symbrachydactylie	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Brachydactyly syndrome type B (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Brachydactyly syndrome type C	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Microcephalus with brachydactyly and kyphoscoliosis syndrome	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	9
Ulna fibula ray defect and brachydactyly syndrome (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	6
Brachydactyly and arterial hypertension syndrome (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Brachydactyly type A2 (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Brachydactyly type A5 (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Brachydactyly type A7	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Brachydactyly with syndactyly Zhao type (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Acro-dermato-ungual-lacrimal-tooth syndrome (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	7
Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	7
Aplasia of fibula and ectrodactyly syndrome (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Heart-hand syndrome Slovenian type (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Coloboma of macula with brachydactyly type B syndrome (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hirschsprung disease with type D brachydactyly syndrome	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	8
Coloboma of macula with brachydactyly type B syndrome (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Karsch-Neugebauer syndrome is a rare syndrome characterised by split-hand and split-foot deformity and ocular abnormalities, mainly a congenital nystagmus.	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	9
Ballard syndrome (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Split hand, split foot malformation with sensorineural hearing loss syndrome	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	8
Paraplegia, brachydactyly, cone-shaped epiphysis syndrome	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	6
Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	10
A rare congenital limb malformation characterised the association of hallux varus with short thumbs and first toes (involving the metacarpals, metatarsals, and distal phalanges; the proximal and middle phalanges are of normal length) and abduction of the affected digits. Intellectual deficit was observed in all reported individuals. There have been no further reports since 1994.	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Camptobrachydactyly (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Mononen-Karnes-Senac syndrome is characterized by skeletal dysplasia associated with finger malformations (brachydactyly with short and abducted thumbs, short index fingers, and markedly short and abducted great toes), variable mild short stature, and mild bowleg with overgrowth of the fibula. It has been described in two males, their mothers, and a maternal aunt. Females are less severely affected than males. X-linked dominant inheritance is suggested.	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Symbrachydactyly	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Intellectual disability, spasticity, ectrodactyly syndrome	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
A rare, genetic, multiple congenital anomalies syndrome characterised by variable expression of the holoprosencephaly (HPE) spectrum in association with ectrodactyly, cleft lip/palate and/or other ectodermal anomalies. Developmental delay of variable severity and endocrine abnormalities are often associated.	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Ectrodactyly polydactyly syndrome (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Tetramelic monodactyly (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Brachydactyly with syndactyly Zhao type (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Brachydactyly syndrome type E	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Ectrodactyly-ectodermal dysplasia-clefting syndrome	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	3
The MMEP syndrome is a congenital syndromic form of split-hand/foot malformation. It is characterized by microcephaly, microphthalmia, ectrodactyly of the lower limbs and prognathism. Intellectual deficit has been reported. MMEP syndrome is considered to be a very rare condition, although the exact prevalence remains unknown. The etiology is not completely understood. Disruption of the sorting nexin 3 gene (SNX3; 6q21) has been shown to play a causative role in MMEP, although this was not confirmed in recent studies.	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Aplasia of fibula and ectrodactyly syndrome (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Microdactyly	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Split hand, split foot malformation with sensorineural hearing loss syndrome	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Mononen-Karnes-Senac syndrome is characterized by skeletal dysplasia associated with finger malformations (brachydactyly with short and abducted thumbs, short index fingers, and markedly short and abducted great toes), variable mild short stature, and mild bowleg with overgrowth of the fibula. It has been described in two males, their mothers, and a maternal aunt. Females are less severely affected than males. X-linked dominant inheritance is suggested.	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ulna fibula ray defect and brachydactyly syndrome (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ballard syndrome (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Camptobrachydactyly (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Microcephalus with brachydactyly and kyphoscoliosis syndrome	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Heart-hand syndrome Slovenian type (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hirschsprung disease with type D brachydactyly syndrome	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Brachydactyly and arterial hypertension syndrome (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Paraplegia, brachydactyly, cone-shaped epiphysis syndrome	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Acro-dermato-ungual-lacrimal-tooth syndrome (disorder)	Finding site	True	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Juvenile reactive arthritis triad	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Oral lesion co-occurrent with reactive arthritis triad	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	7
Circinate vulvovaginitis due to Reiter's disease	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	7
Circinate balanitis co-occurrent with reactive arthritis triad (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	6
Nail dystrophy co-occurrent with reactive arthritis triad (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	6
Axial spondyloarthritis (disorder)	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Ankylosing spondylitis co-occurrent with anterior uveitis	Finding site	False	Entire digit	Inferred relationship	Existential restriction modifier (core metadata concept)	6

Start Page 2 of 3 End

Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
478304010	Entire digit	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
744747016	Entire digit (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
478303016	Digit	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
478304010	Entire digit	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
478304010	Entire digit	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
744747016	Entire digit (body structure)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
744747016	Entire digit (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core