|
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 |
