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733625003: 48,XYYY syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3472819016 48,XYYY syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3472820010 48,XYYY syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
48,XYYY syndrome Is a Anomaly of chromosome Y true Inferred relationship Existential restriction modifier
48,XYYY syndrome Is a Sex chromosome abnormality - male phenotype true Inferred relationship Existential restriction modifier
48,XYYY syndrome Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
48,XYYY syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
48,XYYY syndrome Finding site Sex chromosome Y true Inferred relationship Existential restriction modifier 1
48,XYYY syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
48,XYYY syndrome Associated morphology Aneuploidy true Inferred relationship Existential restriction modifier 1
48,XYYY syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
48,XYYY syndrome Is a Sex chromosome aneuploidy true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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