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205693008: XY, female phenotype (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
315451010 XY, female phenotype en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
591096016 XY, female phenotype (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
315451010 XY, female phenotype en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
591096016 XY, female phenotype (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
591096016 XY, female phenotype (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
XY, female phenotype Is a Sex chromosome abnormality - female phenotype true Inferred relationship Existential restriction modifier (core metadata concept)
XY, female phenotype Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
XY, female phenotype Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
XY, female phenotype Finding site Sex chromosome false Inferred relationship Existential restriction modifier (core metadata concept) 1
XY, female phenotype Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
XY, female phenotype Finding site Sex chromosome false Inferred relationship Existential restriction modifier (core metadata concept) 1
XY, female phenotype Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
XY, female phenotype Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
XY, female phenotype Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier (core metadata concept) 1
XY, female phenotype Finding site Sex chromosome true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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