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890356003: Postaxial polydactyly type A of bilateral little fingers (disorder)


Status: current, 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
4013050017 Congenital duplication of the fifth digit, fully developed with bone and neural tissue. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4012356011 Postaxial polydactyly type A of bilateral little fingers en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4012357019 Bilateral postaxial polydactyly type A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4012358012 Postaxial polydactyly type A of bilateral little fingers (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4012822011 Postaxial polydactyly type A of both little fingers en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
6476861000241112 polydactylie postaxiale de type A 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
6476871000241116 polydactylie postaxiale bilatérale de type A des auriculaires fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6476881000241119 polydactylie postaxiale de type A des deux petits doigts fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6476891000241117 polydactylie postaxiale de type A 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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital duplication of the fifth digit, fully developed with bone and neural tissue. Is a A rare congenital limb malformation characterized by duplication of the fifth digit in a hand or foot, with an extra, well-formed, functional digit at the metacarpophalangeal/metatarsophalangeal or carpometacarpal/tarsometatarsal joint. The malformation can be an isolated finding or be associated with a large number of other anomalies. true Inferred relationship Some
Congenital duplication of the fifth digit, fully developed with bone and neural tissue. Finding site Structure of left little finger true Inferred relationship Some 1
Congenital duplication of the fifth digit, fully developed with bone and neural tissue. Occurrence Congenital true Inferred relationship Some 1
Congenital duplication of the fifth digit, fully developed with bone and neural tissue. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital duplication of the fifth digit, fully developed with bone and neural tissue. Associated morphology Supernumerary structure true Inferred relationship Some 1
Congenital duplication of the fifth digit, fully developed with bone and neural tissue. Associated morphology Supernumerary structure true Inferred relationship Some 2
Congenital duplication of the fifth digit, fully developed with bone and neural tissue. Finding site Structure of right little finger (body structure) true Inferred relationship Some 2
Congenital duplication of the fifth digit, fully developed with bone and neural tissue. Occurrence Congenital true Inferred relationship Some 2
Congenital duplication of the fifth digit, fully developed with bone and neural tissue. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Congenital duplication of the fifth digit, fully developed with bone and neural tissue. Is a Congenital deformity of right finger true Inferred relationship Some
Congenital duplication of the fifth digit, fully developed with bone and neural tissue. Is a Congenital deformity of bilateral upper limbs (disorder) false Inferred relationship Some
Congenital duplication of the fifth digit, fully developed with bone and neural tissue. Is a Congenital deformity of left finger true Inferred relationship Some
Congenital duplication of the fifth digit, fully developed with bone and neural tissue. Is a Bilateral congenital anomaly of upper limbs true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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