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Congenital lipoid adrenal hyperplasia due to STAR deficency
Synonyms: ADRENAL HYPERPLASIA I; Cholesterol Desmolase-Deficient Congenital Adrenal Hyperplasia; Cholesterol monooxygenase (side-chain cleaving) deficiency; Congenital Lipoid Adrenal Hyperplasia; Lipoid adrenal hyperplasia
Gene: STAR
Results:
31 genetic tests from 15 labs with tests matching your search, 1 lab matching in other ways
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Tests names and labsConditionsGenes, analytes, and microbesMethods

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoNeuro Panel

CENTOGENE GmbH and LLC - Guiding Precision Medicine
Germany
18861858
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1101676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Inherited Metabolic Disorders Panel

Dhiti Omics Technologies Private Ltd
India
376317
  • C Sequence analysis of the entire coding region

Beacon Expanded Female Carrier Screening Plus Panel

Fulgent Genetics
United States
716335
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Female Carrier Screening Panel

Fulgent Genetics
United States
690326
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Male Carrier Screening Plus Panel

Fulgent Genetics
United States
661306
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Male Carrier Screening Panel

Fulgent Genetics
United States
636298
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

RenaDx™: Comprehensive Renal Disease Genetics Panel

Precision Medicine Care (PMC®)
United States
469448
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Lipoid adrenal hyperplasia, 201710, Autosomal recessive; LCAH (Congenital adrenal hyperplasia) (STAR gene) (Sequence Analysis-All Coding Exons) (Prenatal)

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

Lipoid adrenal hyperplasia, 201710, Autosomal recessive; LCAH (Congenital adrenal hyperplasia) (STAR gene) (Sequence Analysis-All Coding Exons) (Postnatal)

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

Congenital Adrenal Hyperplasia NGS Panel

Fulgent Genetics
United States
328
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Adrenal Hyperplasia (CAH) Panel

PreventionGenetics, part of Exact Sciences
United States
87
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Horizon 274

Natera, Inc.
United States
265274
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Horizon 274 Male

Natera, Inc.
United States
244254
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Lipoid Congenital Adrenal Hyperplasia

Myriad Genetics, Inc.
United States
11
  • C Sequence analysis of the entire coding region

Horizon 274 Plus TSE

Natera, Inc.
United States
265274
  • E Enzyme assay
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Horizon 274

Natera, Inc.
United States
265274
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ambiguous Genitalia Panel

PreventionGenetics, part of Exact Sciences
United States
12885
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis
31 tests from 15 labs
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❮Page 1 of 2❯
Clinical Exome by Fulgent Genetics
5128 conditions, 4672 genes
CentoNeuro Panel by CENTOGENE GmbH and LLC - Guiding Precision Medicine
1886 conditions, 1858 genes
MitoMet®Plus aCGH Analysis by Baylor Genetics
842 conditions, 637 genes
Nuclear-Mito NGS Panel by Fulgent Genetics
1101 conditions, 676 genes
Inherited Metabolic Disorders Panel by Dhiti Omics Technologies Private Ltd
376 conditions, 317 genes
Beacon Expanded Female Carrier Screening Plus Panel by Fulgent Genetics
716 conditions, 335 genes
Beacon Expanded Female Carrier Screening Panel by Fulgent Genetics
690 conditions, 326 genes
Beacon Expanded Male Carrier Screening Plus Panel by Fulgent Genetics
661 conditions, 306 genes
Beacon Expanded Male Carrier Screening Panel by Fulgent Genetics
636 conditions, 298 genes
RenaDx™: Comprehensive Renal Disease Genetics Panel by Precision Medicine Care (PMC®)
469 conditions, 448 genes
Lipoid adrenal hyperplasia, 201710, Autosomal recessive; LCAH (Congenital adrenal hyperplasia) (STAR gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Lipoid adrenal hyperplasia, 201710, Autosomal recessive; LCAH (Congenital adrenal hyperplasia) (STAR gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Congenital Adrenal Hyperplasia NGS Panel by Fulgent Genetics
32 conditions, 8 genes
Congenital Adrenal Hyperplasia (CAH) Panel by PreventionGenetics, part of Exact Sciences
8 conditions, 7 genes
Horizon 274 by Natera, Inc.
265 conditions, 274 genes
Horizon 274 Male by Natera, Inc.
244 conditions, 254 genes
Lipoid Congenital Adrenal Hyperplasia by Myriad Genetics, Inc.
1 condition, 1 gene
Horizon 274 Plus TSE by Natera, Inc.
265 conditions, 274 genes
Horizon 274 by Natera, Inc.
265 conditions, 274 genes
Ambiguous Genitalia Panel by PreventionGenetics, part of Exact Sciences
128 conditions, 85 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.