FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

254281006: Turner's phenotype - ring chromosome karyotype (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
378515019 Turner's phenotype - ring chromosome karyotype en Synonym Active Entire term case sensitive SNOMED CT core module
645152012 Turner's phenotype - ring chromosome karyotype (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
2838922011 Turner phenotype - ring chromosome karyotype en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Turner's phenotype - ring chromosome karyotype Is a Turner syndrome true Inferred relationship Existential restriction modifier
Turner's phenotype - ring chromosome karyotype Finding site Testis structure false Inferred relationship Existential restriction modifier
Turner's phenotype - ring chromosome karyotype Occurrence Congenital false Inferred relationship Existential restriction modifier
Turner's phenotype - ring chromosome karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Turner's phenotype - ring chromosome karyotype Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Turner's phenotype - ring chromosome karyotype Finding site Ovarian structure false Inferred relationship Existential restriction modifier
Turner's phenotype - ring chromosome karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
Turner's phenotype - ring chromosome karyotype Associated morphology Chromosomal morphology false Inferred relationship Existential restriction modifier 2
Turner's phenotype - ring chromosome karyotype Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Turner's phenotype - ring chromosome karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Turner's phenotype - ring chromosome karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
Turner's phenotype - ring chromosome karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Turner's phenotype - ring chromosome karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
Turner's phenotype - ring chromosome karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Turner's phenotype - ring chromosome karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
Turner's phenotype - ring chromosome karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Turner's phenotype - ring chromosome karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
Turner's phenotype - ring chromosome karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 2
Turner's phenotype - ring chromosome karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Turner's phenotype - ring chromosome karyotype Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Turner's phenotype - ring chromosome karyotype Associated morphology Chromosomal morphology false Inferred relationship Existential restriction modifier
Turner's phenotype - ring chromosome karyotype Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Turner's phenotype - ring chromosome karyotype Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Turner's phenotype - ring chromosome karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Turner's phenotype - ring chromosome karyotype Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Turner's phenotype - ring chromosome karyotype Associated morphology Chromosomal morphology true Inferred relationship Existential restriction modifier 2
Turner's phenotype - ring chromosome karyotype 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

Back to Start