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205686009: Karyotype 46, X iso (Xq) (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
315437010 Karyotype 46, X iso (Xq) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
591088014 Karyotype 46, X iso (Xq) (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
315437010 Karyotype 46, X iso (Xq) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
591088014 Karyotype 46, X iso (Xq) (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4886421000241113 cariotype 46, X, iso Xq fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4886421000241113 cariotype 46, X, iso Xq fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

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

This concept is not in any reference sets

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