FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

890357007: Postaxial polydactyly type B of bilateral little fingers (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
4012824012 Congenital duplication of the fifth digit, rudimentary, non-functioning or soft tissue. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4012359016 Postaxial polydactyly type B of bilateral little fingers en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4012360014 Postaxial polydactyly type B of bilateral little fingers (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4012361013 Bilateral postaxial polydactyly type B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4012823018 Postaxial polydactyly type B of both little fingers en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
6476901000241116 polydactylie postaxiale de type B du cinquième doigt des deux mains fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6476911000241119 polydactylie postaxiale bilatérale de type B des auriculaires fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6476921000241114 polydactylie postaxiale de type B des deux doigts V des mains fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6476931000241111 polydactylie postaxiale de type B des deux petits doigts fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital duplication of the fifth digit, rudimentary, non-functioning or soft tissue. Is a A rare congenital limb malformation characterized by duplication of the fifth digit in a hand or foot, the sixth digit being rudimentary, poorly developed, and non-functional, frequently consisting of additional soft tissue on a pedicle. The anomaly can be unilateral or bilateral. true Inferred relationship Some
Congenital duplication of the fifth digit, rudimentary, non-functioning or soft tissue. Finding site Structure of left little finger true Inferred relationship Some 1
Congenital duplication of the fifth digit, rudimentary, non-functioning or soft tissue. Occurrence Congenital true Inferred relationship Some 1
Congenital duplication of the fifth digit, rudimentary, non-functioning or soft tissue. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital duplication of the fifth digit, rudimentary, non-functioning or soft tissue. Associated morphology Supernumerary structure true Inferred relationship Some 1
Congenital duplication of the fifth digit, rudimentary, non-functioning or soft tissue. Associated morphology Supernumerary structure true Inferred relationship Some 2
Congenital duplication of the fifth digit, rudimentary, non-functioning or soft tissue. Finding site Structure of right little finger (body structure) true Inferred relationship Some 2
Congenital duplication of the fifth digit, rudimentary, non-functioning or soft tissue. Occurrence Congenital true Inferred relationship Some 2
Congenital duplication of the fifth digit, rudimentary, non-functioning or soft tissue. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Congenital duplication of the fifth digit, rudimentary, non-functioning or soft tissue. Is a Congenital deformity of right finger true Inferred relationship Some
Congenital duplication of the fifth digit, rudimentary, non-functioning or soft tissue. Is a Congenital deformity of bilateral upper limbs (disorder) false Inferred relationship Some
Congenital duplication of the fifth digit, rudimentary, non-functioning or soft tissue. Is a Congenital deformity of left finger true Inferred relationship Some
Congenital duplication of the fifth digit, rudimentary, non-functioning or soft tissue. Is a Bilateral congenital anomaly of upper limbs true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

Back to Start