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Gene

AMH-anti-Mullerian hormone
Also know as: MIF, MIS; GeneID:268; Location:19p13.3;
Associated condition:
Results:
32 genetic tests from 19 labs with tests matching your search, 2 labs matching in other ways
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Tests names and labsConditionsGenes, analytes, and microbesMethods

AMH Gene Persistent Mullerian duct syndrome type 1 NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Invitae Disorders of Sex Development Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
8853
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Persistent Mullerian duct syndrome, type I, 261550, Autosomal recessive (Persistent Müllerian duct syndrome) (AMH gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

qGenEx Sex development disorders

Quantitative Genomic Medicine Laboratories, SL
Spain
4548
  • C Sequence analysis of the entire coding region

Differences in sexual development panel

CGC Genetics, Unilabs
Portugal
1100
  • C Sequence analysis of the entire coding region

Exome Panel Sequencing and CNVs

Laboratorio de Genetica Clinica SL
Spain
1105
  • E Sequence analysis of select exons

Exome Panel Sequencing and CNVs

Laboratorio de Genetica Clinica SL
Spain
1311
  • E Sequence analysis of select exons

TYPE 1: Sanger sequencing of AMH

Laboratorio de Genetica Clinica SL
Spain
11
  • E Sequence analysis of select exons

Exome Panel Sequencing and CNVs

Laboratorio de Genetica Clinica SL
Spain
1687
  • E Sequence analysis of select exons

Exome Panel Sequencing and CNVs

Laboratorio de Genetica Clinica SL
Spain
1303
  • E Sequence analysis of select exons

NGS Disorder of sex development DSD

Amsterdam UMC Genome Diagnostics, Amsterdam University Medical Center
Netherlands
185
  • C Sequence analysis of the entire coding region

Persistent Mullerian duct syndrome type I (sequence analysis of AMH gene)

CGC Genetics, Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

AMH Genetic Analysis

Duzen Laboratories, Duzen BBAGUAS
Turkey
11
  • C Sequence analysis of the entire coding region

Gender Development Disorder

Genetiks Genetic Diagnosis Center, Genetic Diseases Evaluation Center
Turkey
11
  • C Sequence analysis of the entire coding region

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Female Infertility panel

Genetic Services Laboratory, University of Chicago
United States
1093
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Custom XomeDx Slice – Differences of Sex Development (Proband Only)

GeneDx
United States
21112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Prenatal Known Familial Mutation

GeneDx
United States
11716
  • D Deletion/duplication analysis
  • T Targeted variant analysis

Custom XomeDxSlice (2-150 Genes, Proband Only)

GeneDx
United States
11718
  • D Deletion/duplication analysis
  • 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
32 tests from 19 labs
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Page 1 of 2
Invitae Disorders of Sex Development Panel by Labcorp Genetics (formerly Invitae), LabCorp
88 conditions, 53 genes
qGenEx Sex development disorders by Quantitative Genomic Medicine Laboratories, SL
45 conditions, 48 genes
Exome Panel Sequencing and CNVs by Laboratorio de Genetica Clinica SL
1 condition, 105 genes
Exome Panel Sequencing and CNVs by Laboratorio de Genetica Clinica SL
1 condition, 311 genes
TYPE 1: Sanger sequencing of AMH by Laboratorio de Genetica Clinica SL
1 condition, 1 gene
Exome Panel Sequencing and CNVs by Laboratorio de Genetica Clinica SL
1 condition, 687 genes
Exome Panel Sequencing and CNVs by Laboratorio de Genetica Clinica SL
1 condition, 303 genes
NGS Disorder of sex development DSD by Amsterdam UMC Genome Diagnostics, Amsterdam University Medical Center
1 condition, 85 genes
AMH Genetic Analysis by Duzen Laboratories, Duzen BBAGUAS
1 condition, 1 gene
Gender Development Disorder by Genetiks Genetic Diagnosis Center, Genetic Diseases Evaluation Center
1 condition, 1 gene
Female Infertility panel by Genetic Services Laboratory, University of Chicago
10 conditions, 93 genes

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.