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715720006: brachydactylie type A1 (aandoening)


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
6254071000146119 brachydactylie type A1 nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6254081000146117 brachydactylie type A1 (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7016311000146119 brachydactylie type Farabee nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Brachydactyly type A1 (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Brachydactyly type A1 (disorder) Is a Brachyphalangia true Inferred relationship Some
Brachydactyly type A1 (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Brachydactyly type A1 (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Brachydactyly type A1 (disorder) Associated morphology Abnormally short growth true Inferred relationship Some 1
Brachydactyly type A1 (disorder) Occurrence Congenital true Inferred relationship Some 1
Brachydactyly type A1 (disorder) Finding site Phalanx structure false Inferred relationship Some 1
Brachydactyly type A1 (disorder) Is a Congenital anomaly of skeletal bone false Inferred relationship Some
Brachydactyly type A1 (disorder) Is a deformiteit van bot (aandoening) false Inferred relationship Some
Brachydactyly type A1 (disorder) Is a Congenital anomaly of digit (disorder) false Inferred relationship Some
Brachydactyly type A1 (disorder) Is a Longitudinal deficiency of part of limb (disorder) false Inferred relationship Some
Brachydactyly type A1 (disorder) Associated morphology Abnormally short growth false Inferred relationship Some 2
Brachydactyly type A1 (disorder) Occurrence Congenital false Inferred relationship Some 2
Brachydactyly type A1 (disorder) Finding site Entire phalanx false Inferred relationship Some 2
Brachydactyly type A1 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Brachydactyly type A1 (disorder) Finding site Entire phalanx true Inferred relationship Some 1
Brachydactyly type A1 (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

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