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254280007: Turner's phenotype, partial X deletion karyotype (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
378514015 Turner's phenotype, partial X deletion karyotype en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
645150016 Turner's phenotype, partial X deletion karyotype (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2838081017 Turner phenotype, partial X deletion karyotype en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
378514015 Turner's phenotype, partial X deletion karyotype en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
645150016 Turner's phenotype, partial X deletion karyotype (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
645150016 Turner's phenotype, partial X deletion karyotype (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2838081017 Turner phenotype, partial X deletion karyotype en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5083441000241117 phenotype de Turner,caryotype avec délétion partielle X fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5083441000241117 phenotype de Turner,caryotype avec délétion partielle X 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
Turner's phenotype, partial X deletion karyotype (disorder) Is a Turner syndrome (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Turner's phenotype, partial X deletion karyotype (disorder) Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, partial X deletion karyotype (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Testis structure false Inferred relationship Existential restriction modifier (core metadata concept)
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Ovarian structure false Inferred relationship Existential restriction modifier (core metadata concept)
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, partial X deletion karyotype (disorder) Associated morphology Chromosomal morphology (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, partial X deletion karyotype (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, partial X deletion karyotype (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Turner's phenotype, partial X deletion karyotype (disorder) Associated morphology Chromosomal morphology (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept)
Turner's phenotype, partial X deletion karyotype (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, partial X deletion karyotype (disorder) Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, partial X deletion karyotype (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, partial X deletion karyotype (disorder) Associated morphology Chromosomal morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, partial X deletion karyotype (disorder) Finding site Sex chromosome X (cell structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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