Analyzes directory
Our daily updated online index for laboratory medical analytics is available on this page for reference purposes, downloading or printing. The names of the individual tests /parameters are listed both in German and English in the online index. By entering either the German or English term in the search function you can directly access the relevant parameter.
More detailed information on the individual analyses is however only available in German language. Should you have any questions on sample materials, preanalytics or indication please contact the specific MVZ sectors or send an e-mail.
To request analyzes from abroad, please use this form Clinical Lab Request.
Humangenetik
- Myeloid, atypical chronic myelogenic leukemia, chronic neutrophilic leukemia, NGS panel
- Obesity, NGS panel
- Congenital adrenal hyperplasia, NGS panel
- Oculocutaneous Albinism, NGS panel
- AML / Myeloid, acute myeloid leukemia - prognostic panel 1, NGS
- AML / Myeloid, acute myeloid leukemia - panel 2 other therapeutic options, NGA panel
- AML / Myeloid, acute myeloid leukemia - panel 3 sensitive for sAML and prognostic, NGS panel
- Amyotrophic lateral sclerosis / ALS , NGS panel
- Angelman syndrome, Happy Puppet syndrome
- Arrhythmogenic right ventricular cardiomyopathy (ARVD), NGS panel
- Ataxia with oculomotor apraxia, NGS panel
- ataxia, episodic / EA, NGS panel
- Spinocerebellar Ataxia, autosomal recessive / SCAR - NGS panel
- Autism spectrum disorder / ASD, NGS panel
- Lymphoid, chronic lymphocytic leukemia, prognostic NGS panel
- Bardet-Biedl syndrome, NGS panel
- Bartter syndrome / Gitelman syndrome, NGS panel
- Basalioma, hereditary - NGS panel
- Beckwith-Wiedemann syndrome / BWS - NGS panel
- Benign familial neonatal seizures (BFNS), NGS panel
- Bethlem myopathy, NGS panel
- Breast and ovarian cancer, hereditary - NGS panel
- Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy, NGS panel
- Myeloid, chronic myelomonocytic leukemia: core panel diagnostic and prognostic, NGS
- Cornelia de Lange syndrome / CDLS, NGS panel
- Dilated cardiomyopathy /DCM, NGS panel
- Early infantile epileptic encephalopathy, severe myoclonic epilepsy of infancy, Dravet syndrome - NGS panel
- Dyskinesia, primary ciliary / PCD - NGS panel
- Dystonia, NGS panel
- Fever syndrome, hereditary - NGS panel
- Fraser syndrome, NGS panel
- Early infantile epileptic encephalopathy / EIEE - NGS panel
- Flecked retina syndromes - NGS panel
- Whole Exome Sequencing (WES)
- Primary open angle glaucoma (POAG), adult onset - NGS panel
- Primary open angle glaucoma (POAG) juvenile onset - NGS panel
- Glycine encephalopathy - NGS panel
- Glycogen storage disease / GSD, NGS panel
- Congenital disorder of glycosylation / CDG - NGS panel
- Overgrowth syndromes, NGS panel
- Hemochromatosis, hereditary (NGS panel)
- Hand foot genital syndrome, NGS panel
- Congenital urea cycle defects - NGS panel
- Hermansky-Pudlak syndrome /HPS, NGS panel
- Heart defects, congenital - NGS panel
- Hypercholesterolemia, familial (FH) / Sitosterolemia (extended hypercholesterolemia panel)
- Hypercholesterolemia, familial (FH), frequent types - NGS panel
- Cardiomyopathy, familial hypertrophic, NGS panel
- Hypogonadotropic Hypogonadism, NGS panel
- Pituitary hormone deficiency, hypopituitarism, panhypopituitarism - NGS panel
- Kabuki syndrome - NGS panel
- Cataract, hereditary - NGS panel
- Catecholaminergic polymorphic ventricular tachycardia / CPVT, NGS panel
- Ketogenesis disorders, NGS panel
- Ketolysis disorders, NGS panel
- Analysis of disorders affecting ketone body metabolism and selected other metabolic disorders, NGS panel
- Disorders of ketone body metabolism, NGS panel
- Analysis of ketone body metabolism/glycogen storage diseases and selected other metabolic disorders, NGS panel
- Short stature, idiopathic familial - NGS panel
- Colorectal cancer / HNPCC/ Lynch syndrome, NGS panel
- Creatine deficiency - NGS Panel
- Leber congenital amaurosis (LCA), NGS panel
- Leigh Syndrome / infantile subacute necrotizing encephalopathy, NGS panel
- Leukodystrophy, late onset - NGS panel
- Leukodystrophy, early onset - NGS panel
- Left ventricular noncompaction / LVNC, NGS panel
- Lipodystrophy, congenital generalized - NGS panel
- Lissencephaly, NGS panel
- Long QT Syndrome, NGS panel
- Lymphoid, unclear disease entity - NGS panel
- Gastric cancer, hereditary - NGS panel
- Macrocephaly, NGS panel
- Malignant hyperthermia, NGS panel
- Myeloid, myeloproliferative neoplasia, systemic mastocytosis SM, AHN panel, NGS
- Myeloid, myeloproliferative neoplasia, systemic mastocytosis SM, prognostic panel small, NGS panel
- Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH), NGS panel
- Myeloid, myelodysplastic syndrome with isolated del(5q), markers with therapeutic relevance, NGS panel
- Myeloid, myelodysplastic/myeloproliferative neoplasms, MDS / MPN overlap, NGS panel
- Myeloid, myelodysplastic syndrome MDS diagnostic, NGS panel
- Myeloid, myelodysplastic syndrome MDS - prognostic markers, NGS panel
- Myeloid, myelodysplastic syndrome MDS, markers with therapeutic relevance, NGS panel
- Meckel Syndrome / MKS, NGS panel
- Melanoma, hereditary - NGS panel
- MELAS (mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes) - NGS panel
- Mental retardation X-linked / MRX - NGS panel
- Mental retardation, autosomal dominant - NGS panel
- Mental retardation, autosomal recessive - NGS panel
- Metabolische Myopathie, NGS-Panel
- Migraine susceptibility, NGS panel
- Migraine, familial hemiplegic - NGS panel
- Mikrophthalmie-Anolphthalmie-Kolombom-Komplex / MAC, NGS-Panel
- Microcephaly, NGS panel
- Mitochondrial hepatic encephalomyopathy, NGS panel
- Mitochondrial cardiomyopathy, NGS panel
- Complete mitochodrial genome, NGS panel
- MODY (Maturity Onset Diabetes of the Young), NGS panel
- Stargardt disease, NGS panel
- Myeloid, myeloproliferative neoplasia, NGS panel 1
- Myeloid, myeloproliferative neoplasia, extended diagnosis panel, NGS panel 2
- Myeloid, myeloproliferative neoplasia, extended prognostic panel, NGS
- Mucopolysaccharidosis, NGS panel
- Muscular dystrophy, NGS panel
- Myasthenic syndrome, myasthenia - NGS panel
- Myeloid, myeloproliferative neoplasia, myelofibrosis prognostic panel according to MIPSS70 or MIPSS70 plus, NGS panel
- Myeloid, myeloproliferative neoplasia, myelofibrosis prognostic panel MIPSS70 or MIPSS70 plus extended, NGS panel
- Myeloid, unclear disease entity, NGS panel
- Myotonia congenita, NGS panel
- Neonatal apneas, NGS panel
- Neonatal diabetes mellitus (NDM) - NGS panel
- Nephrotic syndrome, hereditary - NGS panel
- Neurodegeneration with brain iron accumulation (NBIA) - NGS panel
- Neuropathy, hereditary motor and sensory (HMSN/CMT) - NGS panel
- Congenital anomalies of the kidney and urinary tract / CAKUT - NGS panel
- Kidney disease, polycystic type I/II
- Kidney disease, polycystic dominant / ADPKD - NGS panel
- Kidney disease, polycystic recessive - NGS panel
- Kidney disease, tubulointerstitial autosomal dominant/ADTKD - NGS panel
- Nuclear mitochondriopathy, NGS panel
- Olaparib therapy - NGS panel ( BRCA1 and BRCA2 sequencing)
- Optic atrophy, nuclear type - NGS panel
- Osler-Rendu-Weber disease, NGS panel
- Pancreatic cancer, hereditary - NGS panel
- Pancreatitis, hereditary / PCTT, NGS panel
- Paraganglioma / Pheochromocytoma, NGS panel
- Parkinson disease - NGS panel
- AA / myeloid, Aplastic Anemia - prognostic and therapeutic markers, NGS panel
- Myeloid, myeloproliferative neoplasia, polycythemia vera - prognostic panel, NGS
- Polyposis coli, (attenuated) familial adenomatous (FAP, AFAP) - NGS panel
- Polycystic liver disease, NGS panel
- Pontine and cerebellar hypoplasia, NGS panel
- Porphyria, NGS panel
- Premature ovarian failure (POF), NGS panel
- Primary coenzyme Q10 deficiency (COQ10D), NGS panel
- Progressive familial intrahepatic cholestasis, NGS panel
- Pulmonary arterial hypertension, NGS panel
- Senior-Loken syndrome / juvenile nephronophthisis with Leber amaurosis, NGS panel
- Sensorineural non-syndrome hearing impairment - NGS panel
- Short QT syndrome (SQT), NGS panel
- Silver-Russell syndrome - NGS panel
- Small fiber neuropathy / SFN - NGS panel
- Sotos syndrome, NGS panel
- Spastic paraplegia (SPG), NGS panel
- Storage diseases, lysosomal - NGS panel
- Spherocytosis and Elliptocytosis, hereditary - NGS panel
- Spinal muscular atrophy, adult onset - NGS panel
- Spinocerebellar ataxia (SCA), NGS panel
- Stargardt disease / Macular dystrophy with flecks, NGS panel
- Stickler syndrome, hereditary progressive arthroophthalmopathy - NGS panel
- Thoracic aortic aneurysm/ aortic dissection, NGS panel
- Myeloid, myeloproliferative neoplasia, essential thrombocythemia ET - prognostic panel, NGS
- Trio Whole Exome Sequencing / WES
- Malignant solid tumors - therapy planning, NGS panel
- Cancer predisposition, hereditary - NGS panel
- Cancer predisposition, hereditary - XXL NGS panel
Laboratoriumsmedizin
Mikrobiologie
Requisition form
To request analyzes from abroad, please use this form Clinical Lab Request.
Receipt of material
Anlieferung Probenmaterial durch Patienten
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Anlieferung Probenmaterial durch Fahrdienst/Lieferdienst/Taxi
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Sa.: 7.30-11.30 Uhr
