FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

890438002: Brachydactyly type A3 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4012570010 Brachydactyly type A3 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4012571014 Brachydactyly type A3 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4016120019 A congenital malformation characterised by shortening of the middle phalanx of the fifth finger. Inherited as an autosomal dominant trait. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4016123017 A congenital malformation characterized by shortening of the middle phalanx of the fifth finger. Inherited as an autosomal dominant trait. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5535831000172112 syndrome de brachydactylie de type A3 fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
5535841000172117 brachydactylie de type A3 fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
5535821000172114 brachydactylie type A3 nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Brachydactyly type A3 (disorder) Associated morphology Abnormally short growth true Inferred relationship Some 1
Brachydactyly type A3 (disorder) Finding site Structure of middle phalanx of little finger true Inferred relationship Some 1
Brachydactyly type A3 (disorder) Occurrence Congenital true Inferred relationship Some 1
Brachydactyly type A3 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Brachydactyly type A3 (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Brachydactyly type A3 (disorder) Is a Finding of bone in hand true Inferred relationship Some
Brachydactyly type A3 (disorder) Is a Brachydactyly true Inferred relationship Some
Brachydactyly type A3 (disorder) Is a Congenital anomaly of finger true Inferred relationship Some
Brachydactyly type A3 (disorder) Is a Deformity of bone true Inferred relationship Some
Brachydactyly type A3 (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Brachydactyly type A3 (disorder) Is a Longitudinal deficiency of part of upper limb (disorder) true Inferred relationship Some
Brachydactyly type A3 (disorder) Is a Deformity of hand false Inferred relationship Some
Brachydactyly type A3 (disorder) Is a Congenital anomaly of skeletal bone true Inferred relationship Some
Brachydactyly type A3 (disorder) Is a Finding of musculoskeletal structure of finger true Inferred relationship Some
Brachydactyly type A3 (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Brachydactyly type A3 (disorder) Is a Congenital deformity of hand (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start