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717785002: Coloboma of macula with brachydactyly type B syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3323594014 Coloboma of macula with brachydactyly type B syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3323595010 Coloboma of macula with brachydactyly type B syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3323596011 Sorsby syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401596012 A rare congenital malformation syndrome characterized by the combination of bilateral coloboma of macula with horizontal pendular nystagmus and severe visual loss, and brachydactyly type B. The hand and feet defects comprise of shortening of the middle and terminal phalanges of the second to fifth digits, hypoplastic or absent nails (congenital anonychia), broad or bifid thumbs and halluces, syndactyly and flexion deformities of the joints of some digits. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401597015 A rare congenital malformation syndrome characterised by the combination of bilateral coloboma of macula with horizontal pendular nystagmus and severe visual loss, and brachydactyly type B. The hand and feet defects comprise of shortening of the middle and terminal phalanges of the second to fifth digits, hypoplastic or absent nails (congenital anonychia), broad or bifid thumbs and halluces, syndactyly and flexion deformities of the joints of some digits. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3323594014 Coloboma of macula with brachydactyly type B syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3323595010 Coloboma of macula with brachydactyly type B syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3323596011 Sorsby syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3323597019 A malformation syndrome with the combination of bilateral coloboma of macula, horizontal pendular nystagmus, severe visual loss and brachydactyly type B. The hand and feet defects comprise shortening of the middle and terminal phalanges of the second to fifth digits, hypoplastic or absent nails, broad or bifid thumbs and halluces, syndactyly and flexion deformities of the joints of some digits. Inherited in a dominant manner. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401596012 A rare congenital malformation syndrome characterized by the combination of bilateral coloboma of macula with horizontal pendular nystagmus and severe visual loss, and brachydactyly type B. The hand and feet defects comprise of shortening of the middle and terminal phalanges of the second to fifth digits, hypoplastic or absent nails (congenital anonychia), broad or bifid thumbs and halluces, syndactyly and flexion deformities of the joints of some digits. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401597015 A rare congenital malformation syndrome characterised by the combination of bilateral coloboma of macula with horizontal pendular nystagmus and severe visual loss, and brachydactyly type B. The hand and feet defects comprise of shortening of the middle and terminal phalanges of the second to fifth digits, hypoplastic or absent nails (congenital anonychia), broad or bifid thumbs and halluces, syndactyly and flexion deformities of the joints of some digits. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
601211000274111 Sorsby-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3397271001000115 Makula-Kolobom - Brachydaktylie Typ B de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
878471000172115 syndrome de colobome maculaire-brachydactylie type B fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1006071000172116 syndrome de Sorsby fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
878471000172115 syndrome de colobome maculaire-brachydactylie type B fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1006071000172116 syndrome de Sorsby fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
601211000274111 Sorsby-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3397271001000115 Makula-Kolobom - Brachydaktylie Typ B de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Coloboma of macula with brachydactyly type B syndrome (disorder) Is a Congenital anomaly of macula false Inferred relationship Existential restriction modifier (core metadata concept)
Coloboma of macula with brachydactyly type B syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Coloboma of macula with brachydactyly type B syndrome (disorder) Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
Coloboma of macula with brachydactyly type B syndrome (disorder) Is a Congenital ocular coloboma false Inferred relationship Existential restriction modifier (core metadata concept)
Coloboma of macula with brachydactyly type B syndrome (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Coloboma of macula with brachydactyly type B syndrome (disorder) Is a Brachydactyly syndrome type B (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Coloboma of macula with brachydactyly type B syndrome (disorder) Associated morphology Abnormally short growth true Inferred relationship Existential restriction modifier (core metadata concept) 3
Coloboma of macula with brachydactyly type B syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Coloboma of macula with brachydactyly type B syndrome (disorder) Finding site Entire digit true Inferred relationship Existential restriction modifier (core metadata concept) 3
Coloboma of macula with brachydactyly type B syndrome (disorder) Associated morphology Congenital failure of fusion false Inferred relationship Existential restriction modifier (core metadata concept) 4
Coloboma of macula with brachydactyly type B syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Coloboma of macula with brachydactyly type B syndrome (disorder) Finding site Macula lutea structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Coloboma of macula with brachydactyly type B syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
Coloboma of macula with brachydactyly type B syndrome (disorder) Associated morphology Abnormally short growth false Inferred relationship Existential restriction modifier (core metadata concept) 5
Coloboma of macula with brachydactyly type B syndrome (disorder) Finding site Entire digit false Inferred relationship Existential restriction modifier (core metadata concept) 5
Coloboma of macula with brachydactyly type B syndrome (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
Coloboma of macula with brachydactyly type B syndrome (disorder) Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Coloboma of macula with brachydactyly type B syndrome (disorder) Associated morphology Developmental failure of fusion (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Coloboma of macula with brachydactyly type B syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Coloboma of macula with brachydactyly type B syndrome (disorder) Finding site Macula lutea structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Coloboma of macula with brachydactyly type B syndrome (disorder) Is a Congenital coloboma of macula lutea (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Coloboma of macula with brachydactyly type B syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Coloboma of macula with brachydactyly type B syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Coloboma of macula with brachydactyly type B syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Coloboma of macula with brachydactyly type B syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Coloboma of macula with brachydactyly type B syndrome (disorder) Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Coloboma of macula with brachydactyly type B syndrome (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Coloboma of macula with brachydactyly type B syndrome (disorder) Finding site Macula lutea structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Coloboma of macula with brachydactyly type B syndrome (disorder) Associated morphology Developmental failure of fusion (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Coloboma of macula with brachydactyly type B syndrome (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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