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

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2838081017 Turner phenotype, partial X deletion karyotype en Synonym Active Case sensitive SNOMED CT core
378514015 Turner's phenotype, partial X deletion karyotype en Synonym Active Case sensitive SNOMED CT core
645150016 Turner's phenotype, partial X deletion karyotype (disorder) en Fully specified name Active Case sensitive SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Turner's phenotype, partial X deletion karyotype Finding site Ovarian structure false Inferred relationship Some
Turner's phenotype, partial X deletion karyotype Finding site Sex chromosome X false Inferred relationship Some 2
Turner's phenotype, partial X deletion karyotype Associated morphology Chromosomal morphology false Inferred relationship Some 2
Turner's phenotype, partial X deletion karyotype Associated morphology Congenital anomaly false Inferred relationship Some 1
Turner's phenotype, partial X deletion karyotype Finding site Sex chromosome X false Inferred relationship Some 1
Turner's phenotype, partial X deletion karyotype Finding site Sex chromosome X false Inferred relationship Some 2
Turner's phenotype, partial X deletion karyotype Finding site Sex chromosome X false Inferred relationship Some 1
Turner's phenotype, partial X deletion karyotype Finding site Sex chromosome X false Inferred relationship Some 2
Turner's phenotype, partial X deletion karyotype Finding site Sex chromosome X false Inferred relationship Some 1
Turner's phenotype, partial X deletion karyotype Finding site Sex chromosome X false Inferred relationship Some 2
Turner's phenotype, partial X deletion karyotype Finding site Sex chromosome X false Inferred relationship Some 2
Turner's phenotype, partial X deletion karyotype Finding site Sex chromosome X false Inferred relationship Some 1
Turner's phenotype, partial X deletion karyotype Finding site Sex chromosome X false Inferred relationship Some 2
Turner's phenotype, partial X deletion karyotype Finding site Sex chromosome X false Inferred relationship Some 1
Turner's phenotype, partial X deletion karyotype Is a Turner syndrome true Inferred relationship Some
Turner's phenotype, partial X deletion karyotype Associated morphology Congenital anomaly false Inferred relationship Some
Turner's phenotype, partial X deletion karyotype Associated morphology Chromosomal morphology false Inferred relationship Some
Turner's phenotype, partial X deletion karyotype Occurrence Congenital false Inferred relationship Some 1
Turner's phenotype, partial X deletion karyotype Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Some 1
Turner's phenotype, partial X deletion karyotype Finding site Sex chromosome X false Inferred relationship Some 1
Turner's phenotype, partial X deletion karyotype Occurrence Congenital true Inferred relationship Some 2
Turner's phenotype, partial X deletion karyotype Associated morphology Chromosomal morphology true Inferred relationship Some 2
Turner's phenotype, partial X deletion karyotype Finding site Sex chromosome X true Inferred relationship Some 2
Turner's phenotype, partial X deletion karyotype Associated morphology Alteration of chromosome structure false Inferred relationship Some
Turner's phenotype, partial X deletion karyotype Finding site Sex chromosome X false Inferred relationship Some 1
Turner's phenotype, partial X deletion karyotype Occurrence Congenital false Inferred relationship Some
Turner's phenotype, partial X deletion karyotype Finding site Testis structure false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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