Diagenom GmbH

Personnel

Director: Hagen Pommerenke, PhD, Lab Director
Phone: +49 381 44022410
Fax: +49 381 44022419
Email: [email protected]
Douglas Friday, Laboratory Contact
Phone: +49 381 44022410
Fax: +49 381 44022419
Email: [email protected]
Goran Matic, MD, Genetic Counselor
Phone: +49 381 44022410
Fax: +49 381 44022419
Email: [email protected]
Michael Steiner, MD, Genetic Counselor
Phone: +49 381 44022410
Fax: +49 381 44022419
Email: [email protected]
Stefan Weiss, PhD, Laboratory Contact
Phone: +49 381 44022410
Fax: +49 381 44022419
Email: [email protected]

Conditions and tests

58 conditions/phenotypes with 58 tests
Enter text to narrow down the list

3 beta-Hydroxysteroid dehydrogenase deficiency1 test
Acute intermittent porphyria1 test
Amyotrophic neuralgia1 test
Beckwith-Wiedemann syndrome1 test
Bernard-Soulier syndrome, type A1 test
Breast-ovarian cancer, familial, susceptibility to, 11 test
Breast-ovarian cancer, familial, susceptibility to, 21 test
Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 11 test
Charcot-Marie-Tooth disease type 4B21 test
Charcot-Marie-Tooth disease type 4D1 test
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency1 test
Congenital prothrombin deficiency1 test
Crigler-Najjar syndrome1 test
Deficiency of steroid 11-beta-monooxygenase1 test
Early-onset generalized limb-onset dystonia1 test
Factor V deficiency1 test
Factor VII deficiency1 test
Factor X deficiency1 test
Factor XII deficiency disease1 test
Factor XIII, A subunit, deficiency of1 test
Familial adenomatous polyposis 11 test
Familial adenomatous polyposis 21 test
Familial cold autoinflammatory syndrome 11 test
Familial Mediterranean fever1 test
Familial porphyria cutanea tarda1 test
Freeman-Sheldon syndrome1 test
Gastrointestinal stromal tumor1 test
Gilbert syndrome1 test
Glanzmann thrombasthenia1 test
Hemochromatosis type 11 test
Hemochromatosis type 2A1 test
Hemochromatosis type 2B1 test
Hemochromatosis type 31 test
Hemochromatosis type 41 test
Hereditary antithrombin deficiency1 test
Hereditary coproporphyria1 test
Hereditary factor IX deficiency disease1 test
Hereditary factor VIII deficiency disease1 test
Hereditary factor XI deficiency disease1 test
Hereditary von Willebrand disease1 test
Hyperimmunoglobulin D with periodic fever1 test
Lynch syndrome1 test
Maturity-onset diabetes of the young type 11 test
Maturity-onset diabetes of the young type 21 test
Maturity-onset diabetes of the young type 31 test
Multiple endocrine neoplasia, type 11 test
Multiple endocrine neoplasia, type 21 test
Papillary renal cell carcinoma type 11 test
Peutz-Jeghers syndrome1 test
Protoporphyria, erythropoietic, 11 test
Renal cysts and diabetes syndrome1 test
Spinocerebellar ataxia type 51 test
Thrombophilia due to protein C deficiency, autosomal dominant1 test
Thrombophilia due to protein S deficiency, autosomal dominant1 test
TNF receptor-associated periodic fever syndrome (TRAPS)1 test
Variegate porphyria1 test
Wilson disease1 test
X-linked lymphoproliferative disease due to SH2D1A deficiency1 test

List of services

Clinical Testing/Confirmation of Mutations Identified Previously

List of certifications/licenses

Certifications

ISO15189, Number: D-ML-18903-01-00

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.