LP19730-8
Kallmann syndrome gene
Active
Reference Information
| Type | Source | Reference |
|---|---|---|
| Webcontent | Online Mendelian Inheritance in Man®Copyright OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University. | Link to OMIM |
Basic Part Properties
- Part Name
- Kallmann syndrome gene
- Part Display Name
- Kallmann syndrome gene
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2000-05-04
- Construct for LOINC Short Name
- KMS gene
LOINC Terminology Service (API) using HL7® FHIR® Get Info
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Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| zh-CN | Chinese (China) | 卡尔曼综合征基因 Synonyms: de Morsier 发育不良嗅觉生殖器病; |
| et-EE | Estonian (Estonia) | Kallmani sündroomi geen |
| es-ES | Spanish (Spain) | Gen del síndrome de Kallman |
| it-IT | Italian (Italy) | Sindrome di Kallmann, gene Synonyms: Gene della sindrome di Kallmann |
| tr-TR | Turkish (Turkey) | Kallman sendromu geni |
| ru-RU | Russian (Russian Federation) | Кальмана синдром ген Synonyms: Ген синдрома Кальмана |
| nl-NL | Dutch (Netherlands) | Kallman-syndroom gen |
| fr-FR | French (France) | Syndrome de Kallmann gène |
| pl-PL | Polish (Poland) | Gen zespołu Kallmanna |
| el-GR | Greek (Greece) | Γονίδιο συνδρόμου Kallmann Synonyms: Γονίδιο συνδρόμου Kallmann |
LOINC Copyright
Copyright © Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://