FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

405769009: Klinefelter's syndrome, XXY (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2004. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2149599019 Klinefelter's syndrome, XXY (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
2157545011 Klinefelter's syndrome, XXY en Synonym Active Entire term case sensitive SNOMED CT core module
2163148019 XXY syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
2163150010 Klinefelter's syndrome karyotype 47 XXY en Synonym Active Entire term case sensitive SNOMED CT core module
2163151014 XXY Klinefelter's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
2838565019 Klinefelter syndrome, XXY 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
Klinefelter's syndrome, XXY Is a Klinefelter's syndrome false Inferred relationship Existential restriction modifier
Klinefelter's syndrome, XXY Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Klinefelter's syndrome, XXY Occurrence Congenital false Inferred relationship Existential restriction modifier
Klinefelter's syndrome, XXY Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome, XXY Is a Klinefelter's syndrome - male with more than two X chromosomes false Inferred relationship Existential restriction modifier
Klinefelter's syndrome, XXY Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome, XXY Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome, XXY Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Klinefelter's syndrome, XXY Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome, XXY Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome, XXY Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome, XXY Is a Klinefelter syndrome true Inferred relationship Existential restriction modifier
Klinefelter's syndrome, XXY Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Klinefelter's syndrome, XXY Associated morphology Alteration of chromosome structure true Inferred relationship Existential restriction modifier 2
Klinefelter's syndrome, XXY 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