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205684007: Turner's phenotype, karyotype normal (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
315435019 Turner's phenotype, karyotype normal en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
591086013 Turner's phenotype, karyotype normal (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2838267014 Turner phenotype, karyotype normal en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
315435019 Turner's phenotype, karyotype normal en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
591086013 Turner's phenotype, karyotype normal (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
591086013 Turner's phenotype, karyotype normal (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2838267014 Turner phenotype, karyotype normal en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4886401000241115 phenotype de Turner,caryotype normal fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4886401000241115 phenotype de Turner,caryotype normal 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
Turner's phenotype, karyotype normal (disorder) Is a Turner syndrome (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Turner's phenotype, karyotype normal (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, karyotype normal (disorder) Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
Turner's phenotype, karyotype normal (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Turner's phenotype, karyotype normal (disorder) Finding site Testis structure false Inferred relationship Existential restriction modifier (core metadata concept)
Turner's phenotype, karyotype normal (disorder) Finding site Ovarian structure false Inferred relationship Existential restriction modifier (core metadata concept)
Turner's phenotype, karyotype normal (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, karyotype normal (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, karyotype normal (disorder) Associated morphology Chromosomal morphology (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, karyotype normal (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, karyotype normal (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, karyotype normal (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, karyotype normal (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, karyotype normal (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, karyotype normal (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, karyotype normal (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, karyotype normal (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, karyotype normal (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, karyotype normal (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, karyotype normal (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Turner's phenotype, karyotype normal (disorder) Associated morphology Chromosomal morphology (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept)
Turner's phenotype, karyotype normal (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, karyotype normal (disorder) Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, karyotype normal (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, karyotype normal (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, karyotype normal (disorder) Associated morphology Chromosomal morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Turner's phenotype, karyotype normal (disorder) 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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