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715720006: Brachydactyly type A1 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3303507017 Brachydactyly type A1 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303508010 Brachydactyly type A1 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303509019 Brachydactyly Farabee type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5401045016 A rare, congenital limb malformation characterized by shortened or underdeveloped middle phalanges of all digits, that are sometimes fused with the terminal phalanges. The proximal phalanges of the thumbs and big toes are also shortened. Short stature in adulthood has been reported in association. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401046015 A rare, congenital limb malformation characterised by shortened or underdeveloped middle phalanges of all digits, that are sometimes fused with the terminal phalanges. The proximal phalanges of the thumbs and big toes are also shortened. Short stature in adulthood has been reported in association. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3303507017 Brachydactyly type A1 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303508010 Brachydactyly type A1 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303509019 Brachydactyly Farabee type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303510012 A congenital malformation with apparent shortness (or absence) of the middle phalanges of all digits and occasional fusion with the terminal phalanges. The proximal phalanges of the thumbs and big toes are short. Tendency to be of short stature in adulthood. Inherited as an autosomal dominant trait. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401045016 A rare, congenital limb malformation characterized by shortened or underdeveloped middle phalanges of all digits, that are sometimes fused with the terminal phalanges. The proximal phalanges of the thumbs and big toes are also shortened. Short stature in adulthood has been reported in association. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401046015 A rare, congenital limb malformation characterised by shortened or underdeveloped middle phalanges of all digits, that are sometimes fused with the terminal phalanges. The proximal phalanges of the thumbs and big toes are also shortened. Short stature in adulthood has been reported in association. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3440561001000111 Brachydaktylie Typ A1 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
937671000172111 brachydactylie type Farabee fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
944571000172119 brachydactylie type A1 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
937671000172111 brachydactylie type Farabee fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
944571000172119 brachydactylie type A1 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3440561001000111 Brachydaktylie Typ A1 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
Brachydactyly type A1 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Brachydactyly type A1 Is a Brachyphalangia true Inferred relationship Existential restriction modifier (core metadata concept)
Brachydactyly type A1 Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Brachydactyly type A1 Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Brachydactyly type A1 Associated morphology Abnormally short growth true Inferred relationship Existential restriction modifier (core metadata concept) 1
Brachydactyly type A1 Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Brachydactyly type A1 Finding site Phalanx structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Brachydactyly type A1 Is a Congenital anomaly of skeletal bone false Inferred relationship Existential restriction modifier (core metadata concept)
Brachydactyly type A1 Is a déformation d'un os false Inferred relationship Existential restriction modifier (core metadata concept)
Brachydactyly type A1 Is a Congenital anomaly of digit false Inferred relationship Existential restriction modifier (core metadata concept)
Brachydactyly type A1 Is a Longitudinal deficiency of part of limb (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Brachydactyly type A1 Associated morphology Abnormally short growth false Inferred relationship Existential restriction modifier (core metadata concept) 2
Brachydactyly type A1 Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Brachydactyly type A1 Finding site Entire phalanx false Inferred relationship Existential restriction modifier (core metadata concept) 2
Brachydactyly type A1 Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Brachydactyly type A1 Finding site Entire phalanx true Inferred relationship Existential restriction modifier (core metadata concept) 1
Brachydactyly type A1 Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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