FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

50749006: Double Y syndrome (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
84580015 Double Y syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
84581016 XYY syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
788571019 Double Y syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
4572065017 Y disomy en Synonym Active Entire term case sensitive SNOMED CT core module
4572066016 47,XYY 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
Double Y syndrome Is a Sex chromosome abnormality - male phenotype true Inferred relationship Existential restriction modifier
Double Y syndrome Is a Anomaly of chromosome Y true Inferred relationship Existential restriction modifier
Double Y syndrome Finding site Sex chromosome Y false Inferred relationship Existential restriction modifier 1
Double Y syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Double Y syndrome Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Double Y syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Double Y syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Double Y syndrome Finding site Sex chromosome Y false Inferred relationship Existential restriction modifier 1
Double Y syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Double Y syndrome Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Double Y syndrome Finding site Sex chromosome Y true Inferred relationship Existential restriction modifier 1
Double Y syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Double Y syndrome Associated morphology Aneuploidy true Inferred relationship Existential restriction modifier 1
Double Y syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Double Y 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

Back to Start