FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

700489002: Sensorineural deafness and male infertility (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2990692017 Sensorineural deafness and male infertility en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2990745014 Deafness infertility syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2990749015 Sensorineural deafness and male infertility (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2990757017 Chromosome 15q15.3 deletion syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2990803015 Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
2990692017 Sensorineural deafness and male infertility en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2990692017 Sensorineural deafness and male infertility en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2990745014 Deafness infertility syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2990745014 Deafness infertility syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2990749015 Sensorineural deafness and male infertility (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2990749015 Sensorineural deafness and male infertility (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2990757017 Chromosome 15q15.3 deletion syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2990757017 Chromosome 15q15.3 deletion syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2990803015 Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3450051001000115 Schwerhörigkeit-Infertilitäts-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6498811000241116 syndrome de délétion du chromosome 15q15.3 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6498821000241111 surdité neurosensorielle et infertilité masculine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6498831000241113 syndrome de surdité et infertilité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6498811000241116 syndrome de délétion du chromosome 15q15.3 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6498821000241111 surdité neurosensorielle et infertilité masculine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6498831000241113 syndrome de surdité et infertilité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3450051001000115 Schwerhörigkeit-Infertilitäts-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Is a Male infertility of chromosomal origin true Inferred relationship Existential restriction modifier (core metadata concept)
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Is a Congenital hearing disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Is a Recessive sensorineural hearing loss (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Finding site Inner ear structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Has definitional manifestation Infertile (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Due to Chromosomal disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Interprets Hearing true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Is a Reproductive system hereditary disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 5
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Finding site Male genital structure true Inferred relationship Existential restriction modifier (core metadata concept) 5
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Interprets entité observable fonctionnelle false Inferred relationship Existential restriction modifier (core metadata concept)
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Interprets Reproductive function false Inferred relationship Existential restriction modifier (core metadata concept) 3
Sensorineural deafness and male infertility caused by a deletion of genetic material on the long (q) arm of chromosome 15. Interprets Fertility, function (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start