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Results: 1 to 20 of 31

Tests names and labsConditionsGenes and analytesMethods

Hypogonadotropic hypogonadism

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypogonadotropic Hypogonadism

Amplexa Genetics Amplexa Genetics A/S
Denmark
116
  • S Mutation scanning of the entire coding region

Hypogonadotropic Hypogonadism/Kallmann Panel

PreventionGenetics
United States
3538
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Disorders of Sex Development (DSD) Panel

PreventionGenetics
United States
149158
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Disorders of Sex Development (DSD) and Infertility Panel

PreventionGenetics
United States
191207
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Male Infertility Panel

PreventionGenetics
United States
97107
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Female Infertility Panel

PreventionGenetics
United States
96105
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Idiopathic Hypogonadotropic Hypogonadism (IHH) via the KISS1 Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Endocrine Disorders

Genomics For Life
Australia
1338
  • E Sequence analysis of select exons

NewbornDx Advanced Sequencing Evaluation

Athena Diagnostics Inc
United States
11722
  • C Sequence analysis of the entire coding region

Hypogonadotropic hypogonadism with or without anosmia: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
2424
  • C Sequence analysis of the entire coding region

Kallmann Syndrome and Hypogonadotropic Hypogonadism Sequencing Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
3439
  • C Sequence analysis of the entire coding region

Male Infertility NGS Panel

Fulgent Genetics
United States
7945
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Infertility NGS Panel

Fulgent Genetics
United States
9256
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Female Infertility NGS Panel

Fulgent Genetics
United States
7641
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HYPOGONADOTROPIC HYPOGONADISM WITH ANOSMIA (KALLLMAN SYNDROME) NGS PANEL

Laboratorio de Genetica Clinica SL
Spain
125
  • C Sequence analysis of the entire coding region

Kallmann Syndrome , Panel Massive Sequencing (NGS) 20 Genes

Reference Laboratory Genetics
Spain
2120
  • C Sequence analysis of the entire coding region

Endocrine Disorders: Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
10857
  • D Deletion/duplication analysis

Hypogonadism hypogonadotropic (NGS panel of 26 genes)

CGC Genetics
Portugal
2626
  • C Sequence analysis of the entire coding region

Hypogonadism hypogonadotropic (NGS panel of 26 genes)

CGC Genetics
Portugal
2626
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 31

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

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