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205693008: XY, female phenotype (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
315451010 XY, female phenotype en Synonym Active Case sensitive SNOMED CT core
591096016 XY, female phenotype (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
XY, female phenotype Associated morphology Congenital anomaly false Inferred relationship Some 1
XY, female phenotype Is a Sex chromosome abnormality - female phenotype true Inferred relationship Some
XY, female phenotype Finding site Sex chromosome false Inferred relationship Some 1
XY, female phenotype Associated morphology Congenital anomaly false Inferred relationship Some
XY, female phenotype Occurrence Congenital true Inferred relationship Some 1
XY, female phenotype Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Some 1
XY, female phenotype Finding site Sex chromosome true Inferred relationship Some 1
XY, female phenotype Associated morphology Alteration of chromosome structure false Inferred relationship Some
XY, female phenotype Occurrence Congenital false Inferred relationship Some
XY, female phenotype Finding site Sex chromosome false Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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