J0641

Myoclonic Epilepsy with Ragged Red Fibers, MERFF, molecular diagnostics, special case

1 494,00

J0651

Mitochondrial depletion syndrome, molecular diagnostics, special case

633,00

J0652

Mitochondrial depletion syndrome, biochemical diagnostics

J0661

Alzheimer, early onset/familial, molecular diagnostics, special case

633,00

J0671

Ataxia Telangiectasia, molecular diagnostics, special case

633,00

J0673

Ataxia Telangiectasia, cytogenetic diagnostics

4 613,00

J0681

Charcot-Marie-Tooth neuropathy, molecular diagnostics, special case

1 292,00

J0691

Creutzfeldt-Jakob disease, familial, molecular diagnostics, special case

633,00

J0701

Duchenne, Becker muscular dystrophy, molecular diagnostics, special case

9 011,00

J0710

Familial dysautonomia, molecular diagnostics

411,00

J0720

Dystonia, torsion, molecular diagnostics

816,00

J0730

Facioscapulohumeral muscular dystrophy-1A, molecular diagnostics

1 292,00

J0740

Hereditary Nerve Pressure Palsy, HNPP, molecular diagnostics

1 494,00

J0750

Huntington disease, molecular diagnostics

1 494,00

J0761

Inclusion body myopathy, autosomal recessive, molecular diagnostics, special case

633,00

J0771

Insensitivity to pain, congenital, with anhidrosis, molecular diagnostics, special case

633,00

J0781

LGMD (Limb girdle muscular dystrophy), dysferlin deficiency, molecular diagnostics, special case

633,00

J0790

Myotonic dystrophy, molecular diagnostics

1 494,00

J0801

Neurofibromatosis, type 1, molecular diagnostics, special case

633,00

J0810

Oculopharyngeal muscular dystrophy, molecular diagnostics

1 494,00

J0820

SMA (Spinal Muscular Atrophy), molecular diagnostics

1 494,00

J0830

Spinocerebellar ataxia due to an expansion including Friedrich ataxia, molecular diagnostics

1 494,00

J0840

Adenomatous polyposis coli, molecular diagnostics

7 247,00

J0841

Adenomatous polyposis coli, molecular diagnostics, special case

633,00

J0850

Multiple endocrine neoplasia 2A, molecular diagnostics

1 631,00

J0851

Multiple endocrine neoplasia 2A, molecular diagnostics, special case

633,00

J0860

Retinoblastoma, molecular diagnostics

7 247,00

J0861

Retinoblastoma, molecular diagnostics, special case

633,00

J0870

Von Hippel-Lindau, molecular diagnostics

1 329,00

J0871

Von Hippel-Lindau, molecular diagnostics, special case

633,00

J0881

Adrenal hyperplasia, congenital, 11-beta-hydroxylase deficiency, molecular diagnostics, special case

633,00

J0891

Adrenal hyperplasia, congenital, 17-alpha-hydroxylase deficiency, molecular diagnostics, special case

633,00

J0901

Adrenal hyperplasia, congenital, 21-hydroxylase deficiency, molecular diagnostics, special case

633,00

J0911

Adrenal hypoplasia, congenital, molecular diagnostics, special case

633,00

J0921

Pendred syndrome, molecular diagnostics, special case

633,00

J0931

Persistent hyperinsulinemic hypoglycemia of infancy, molecular diagnostics, special case

633,00

J0941

Combined factor V and VII deficiency, molecular diagnostics, special case

633,00

J0951

Factor V deficiency, molecular diagnostics, special case

633,00

J0961

Factor VII deficiency, molecular diagnostics, special case

633,00

J0971

Factor XI deficiency, molecular diagnostics, special case

633,00

J0981

Factor XIIIA deficiency, molecular diagnostics, special case

633,00

J0991

Fanconi anemia, molecular diagnostics, special case

633,00

J0993

Fanconi anemia, cytogenetic diagnostics

4 613,00

J1001

Hemoglobinopathies alpha, alpha thalassemias, molecular diagnostics, special case

1 919,00

J1011

Hemoglobinopathies beta, beta thalassemias, molecular diagnostics, special case

1 919,00

J1021

Hemophilia A, factor VIII deficiency, molecular diagnostics, special case

633,00

J1031

Hemophilia B, factor IX deficiency, molecular diagnostics, special case

633,00

J1040

Achondroplasia/thanatophoric dwarfism, molecular diagnostics

633,00

J1051

Achromatopsia, molecular diagnostics, special case

633,00

J1061

Albinism, molecular diagnostics, special case

633,00

J1070

Angelman syndrome/Prader Willi, molecular diagnostics

1 292,00

J1081

Autoimmune polyglandular disease, type I, molecular diagnostics, special case

633,00

J1091

Bardet-Biedl syndrome, molecular diagnostics, special case

633,00

J1100

Beckwith-Wiedemann syndrome, molecular diagnostics

1 292,00

J1111

Bloom syndrome, molecular diagnostics, special case

411,00

J1113

Bloom syndrome, cytogenetic diagnostics

4 613,00

J1121

Cockayne syndrome, molecular diagnostics, special case

633,00

J1122

Cockayne syndrome, biochemical diagnostics

6 116,00

J1131

Craniosynostosis, molecular diagnostics, special case

633,00

J1140

Cystic fibrosis, molecular diagnostics

816,00

J1151

Deafness, congenital, molecular diagnostics, special case

633,00

J1161

Epidermolysis Bullosa, congenital, molecular diagnostics, special case

633,00

J1171

Osteopetrosis, recessive, molecular diagnostics, special case

633,00

J1181

Polycystic kidneys, dominant, molecular diagnostics, special case

633,00

J1191

Polycystic kidneys, recessive, molecular diagnostics, special case

633,00

J1203

Roberts syndrome, cytogenetic diagnostics

4 613,00

J1211

Tuberous sclerosis, molecular diagnostics, special case

633,00

J1222

Xeroderma pigmentosum, biochemical diagnostics

6 116,00

J1233

DiGeorge/velocardiofacial syndrome, FISH, cytogenetic diagnostics

1 934,00

J1243

Rubinstein-Taybi syndrome, FISH, cytogenetic diagnostics

1 934,00

J1253

Smith-Magenis syndrome, FISH, cytogenetic diagnostics

1 934,00