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Hypospadias 2, X-linked
Gene: MAMLD1
Results:
17 genetic tests from 11 labs with tests matching your search
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Tests names and labsConditionsGenes, analytes, and microbesMethods

High-Resolution Rapid Microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Rapid microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • D Deletion/duplication analysis
  • H Detection of homozygosity

CentoNeuro Panel

CENTOGENE GmbH and LLC - Guiding Precision Medicine
Germany
18861858
  • D Deletion/duplication analysis
  • C Sequence analysis 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

Hypospadias 2, X-linked, 300758, X-linked recessive; HYSP2 (Familial hypospadias) (MAMLD1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

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

Hypospadias 2, X-linked, 300758, X-linked recessive; HYSP2 (Familial hypospadias) (MAMLD1 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

X-chromosome High Resolution microarray analysis

Pittsburgh Cytogenetics Laboratory, University of Pittsburgh Medical Center
United States
240171
  • D Deletion/duplication analysis

Hypospadias 2, X-linked (sequence analysis of MAMLD1 gene)

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

Hypospadias: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
22
  • C Sequence analysis of the entire coding region

Hypospadias Panel

PreventionGenetics, part of Exact Sciences
United States
15673
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Differences of Sex Development (DSD) Panel

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

Male Infertility Panel

PreventionGenetics, part of Exact Sciences
United States
127137
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Female Infertility Panel

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

46,XY Disorders of Sex Development/Complete Gonadal Dysgenesis Panel

Genetic Services Laboratory, University of Chicago
United States
2739
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MAMLD1 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51274672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
17 tests from 11 labs
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View the list of labs matching your search query.
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High-Resolution Rapid Microarray (CGH and SNP) by Allele Diagnostics
247 conditions, 231 genes
Rapid microarray (CGH and SNP) by Allele Diagnostics
247 conditions, 231 genes
CentoNeuro Panel by CENTOGENE GmbH and LLC - Guiding Precision Medicine
1886 conditions, 1858 genes
Invitae Disorders of Sex Development Panel by Labcorp Genetics (formerly Invitae), LabCorp
88 conditions, 53 genes
Hypospadias 2, X-linked, 300758, X-linked recessive; HYSP2 (Familial hypospadias) (MAMLD1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Hypospadias 2, X-linked, 300758, X-linked recessive; HYSP2 (Familial hypospadias) (MAMLD1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
qGenEx Sex development disorders by Quantitative Genomic Medicine Laboratories, SL
45 conditions, 48 genes
X-chromosome High Resolution microarray analysis by Pittsburgh Cytogenetics Laboratory, University of Pittsburgh Medical Center
240 conditions, 171 genes
Hypospadias 2, X-linked (sequence analysis of MAMLD1 gene) by CGC Genetics, Unilabs
1 condition, 1 gene
Hypospadias: Full gene sequencing panel by CEN4GEN Institute for Genomics and Molecular Diagnostics
2 conditions, 2 genes
Hypospadias Panel by PreventionGenetics, part of Exact Sciences
156 conditions, 73 genes
Differences of Sex Development (DSD) Panel by PreventionGenetics, part of Exact Sciences
149 conditions, 158 genes
Male Infertility Panel by PreventionGenetics, part of Exact Sciences
127 conditions, 137 genes
Female Infertility Panel by PreventionGenetics, part of Exact Sciences
96 conditions, 105 genes
46,XY Disorders of Sex Development/Complete Gonadal Dysgenesis Panel by Genetic Services Laboratory, University of Chicago
27 conditions, 39 genes
MAMLD1 Single Gene by Fulgent Genetics
1 condition, 1 gene
Clinical Exome by Fulgent Genetics
5127 conditions, 4672 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.