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

74398009: XX males (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
123556019 XX males en Synonym Active Entire term case sensitive SNOMED CT core module
814892014 XX males (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1233740010 Male with 46, XX karyotype en Synonym Active Only initial character case insensitive SNOMED CT core module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
XX males Is a Anomaly of chromosome X true Inferred relationship Existential restriction modifier
XX males Is a Sex phenotype-karyotype dissociation syndrome true Inferred relationship Existential restriction modifier
XX males Is a Sex chromosome abnormality - male phenotype true Inferred relationship Existential restriction modifier
XX males Occurrence Congenital false Inferred relationship Existential restriction modifier
XX males Finding site Male structure false Inferred relationship Existential restriction modifier
XX males Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
XX males Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
XX males Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
XX males Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
XX males Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
XX males Occurrence Congenital false Inferred relationship Existential restriction modifier 1
XX males Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
XX males Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
XX males Occurrence Congenital true Inferred relationship Existential restriction modifier 2
XX males Associated morphology Chromosomal morphology true Inferred relationship Existential restriction modifier 2
XX males Finding site Sex chromosome X true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Klinefelter syndrome, male with 46,XX karyotype Is a True XX males Inferred relationship Existential restriction modifier
[X]Other male with 46,XX karyotype Is a False XX males Inferred relationship Existential restriction modifier
[X]Other male with 46,XX karyotype Is a False XX males Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start