FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

236791009: Male infertility of chromosomal origin (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
354909018 Male infertility of chromosomal origin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
625431016 Male infertility of chromosomal origin (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6371831000241118 infertilité chez l'homme d'origine chromosomique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6371841000241111 infertilité masculine d'origine chromosomique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Male infertility of chromosomal origin Is a Congenital male infertility true Inferred relationship Some
Male infertility of chromosomal origin Finding site Entire subdivision of male genital system (body structure) false Inferred relationship Some
Male infertility of chromosomal origin Occurrence Congenital false Inferred relationship Some
Male infertility of chromosomal origin Finding site Male genital structure false Inferred relationship Some
Male infertility of chromosomal origin Due to Chromosomal disorder (disorder) true Inferred relationship Some 2
Male infertility of chromosomal origin Has definitional manifestation Infertile false Inferred relationship Some
Male infertility of chromosomal origin Occurrence Congenital true Inferred relationship Some 1
Male infertility of chromosomal origin Finding site Male genital structure true Inferred relationship Some 1
Male infertility of chromosomal origin Interprets Reproductive function false Inferred relationship Some 3
Male infertility of chromosomal origin Interprets Fertility, function (observable entity) true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Is a True Male infertility of chromosomal origin Inferred relationship Some
Male infertility with teratozoospermia due to single gene mutation is a rare, genetic male infertility due to sperm disorder characterized by the presence of spermatozoa with abnormal morphology, such as macrozoospermia or globozoospermia, in over 85% of sperm, resulting from mutation in a single gene known to cause teratozoospermia. It is a heterogeneous group that includes a wide range of abnormal sperm phenotypes affecting, solely or simultaneously, head, neck, midpiece, and/or tail. Is a False Male infertility of chromosomal origin Inferred relationship Some
A rare genetic male infertility with characteristics of azoospermia resulting from a mutation in a single gene known to cause azoospermia. Sperm morphology may be normal. Is a False Male infertility of chromosomal origin Inferred relationship Some
A rare genetic male infertility due to oligozoospermia (number of sperm in the ejaculate inferior to 15 million/mL) resulting from a mutation in a single gene known to cause oligozoospermia. Sperm morphology may be normal. Is a False Male infertility of chromosomal origin Inferred relationship Some

This concept is not in any reference sets

Back to Start