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205693008: XY, female phenotype (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
315451010 XY, female phenotype en Synonym Active Entire term case sensitive SNOMED CT core module
591096016 XY, female phenotype (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

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
XY, female phenotype Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
XY, female phenotype Occurrence Congenital false Inferred relationship Existential restriction modifier
XY, female phenotype Finding site Sex chromosome false Inferred relationship Existential restriction modifier 1
XY, female phenotype Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
XY, female phenotype Finding site Sex chromosome false Inferred relationship Existential restriction modifier 1
XY, female phenotype Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
XY, female phenotype Occurrence Congenital true Inferred relationship Existential restriction modifier 1
XY, female phenotype Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier 1
XY, female phenotype Finding site Sex chromosome true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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