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205686009: Karyotype 46, X iso (Xq) (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
315437010 Karyotype 46, X iso (Xq) en Synonym Active Only initial character case insensitive SNOMED CT core module
591088014 Karyotype 46, X iso (Xq) (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Karyotype 46, X iso (Xq) Is a Turner syndrome true Inferred relationship Existential restriction modifier
Karyotype 46, X iso (Xq) Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Karyotype 46, X iso (Xq) Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Karyotype 46, X iso (Xq) Occurrence Congenital false Inferred relationship Existential restriction modifier
Karyotype 46, X iso (Xq) Finding site Testis structure false Inferred relationship Existential restriction modifier
Karyotype 46, X iso (Xq) Finding site Ovarian structure false Inferred relationship Existential restriction modifier
Karyotype 46, X iso (Xq) Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
Karyotype 46, X iso (Xq) Associated morphology Chromosomal morphology false Inferred relationship Existential restriction modifier 2
Karyotype 46, X iso (Xq) Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Karyotype 46, X iso (Xq) Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Karyotype 46, X iso (Xq) Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
Karyotype 46, X iso (Xq) Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
Karyotype 46, X iso (Xq) Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Karyotype 46, X iso (Xq) Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Karyotype 46, X iso (Xq) Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
Karyotype 46, X iso (Xq) Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Karyotype 46, X iso (Xq) Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
Karyotype 46, X iso (Xq) Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Karyotype 46, X iso (Xq) Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
Karyotype 46, X iso (Xq) Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Karyotype 46, X iso (Xq) Associated morphology Chromosomal morphology false Inferred relationship Existential restriction modifier
Karyotype 46, X iso (Xq) Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Karyotype 46, X iso (Xq) Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Karyotype 46, X iso (Xq) Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Karyotype 46, X iso (Xq) Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Karyotype 46, X iso (Xq) Associated morphology Chromosomal morphology true Inferred relationship Existential restriction modifier 2
Karyotype 46, X iso (Xq) Finding site Sex chromosome X true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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