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50749006: Double Y syndrome (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
84580015 Double Y syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
84581016 XYY syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
788571019 Double Y syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4572065017 Y disomy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4572066016 47,XYY syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4572067013 A sex chromosome aneuploidy where males receive an additional Y chromosome, and with clinical characteristics of tall stature evident from childhood, macrocephaly, facial features (mild hypertelorism, low set ears, a mildly flat malar region), speech delay and an increased risk for social and emotional difficulties, attention deficit hyperactive disorder and autistic spectrum disorder. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
84580015 Double Y syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
84581016 XYY syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
788571019 Double Y syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4572065017 Y disomy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4572066016 47,XYY syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4572067013 A sex chromosome aneuploidy where males receive an additional Y chromosome, and with clinical characteristics of tall stature evident from childhood, macrocephaly, facial features (mild hypertelorism, low set ears, a mildly flat malar region), speech delay and an increased risk for social and emotional difficulties, attention deficit hyperactive disorder and autistic spectrum disorder. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3415521001000115 47,XYY-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4555591000241113 syndrome du double Y fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4555591000241113 syndrome du double Y fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3415521001000115 47,XYY-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained 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 (core metadata concept)
Double Y syndrome Is a Anomaly of chromosome Y true Inferred relationship Existential restriction modifier (core metadata concept)
Double Y syndrome Finding site Sex chromosome Y false Inferred relationship Existential restriction modifier (core metadata concept) 1
Double Y syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Double Y syndrome Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
Double Y syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Double Y syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Double Y syndrome Finding site Sex chromosome Y false Inferred relationship Existential restriction modifier (core metadata concept) 1
Double Y syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Double Y syndrome Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier (core metadata concept) 1
Double Y syndrome Finding site Sex chromosome Y true Inferred relationship Existential restriction modifier (core metadata concept) 1
Double Y syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Double Y syndrome Associated morphology Aneuploidy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Double Y syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Double Y syndrome Is a Sex chromosome aneuploidy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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