D9221
Deep sedation/general anesthesia, for complex dental procedure - more than one hour
1 962,00
D9230
Analgesia, including nitrous, excluding dental treatment
320,00
J0011
Methylglutaconic aciduria, molecular diagnostics, special case
633,00
J0021
Adrenoleukodystrophy X-linked, molecular diagnostics, special case
J0031
Canavan disease, molecular diagnostics, special case
J0041
Carnitine Palmitoyl Tranferase, molecular diagnostics, special case
J0051
Cystinuria, molecular diagnostics, special case
J0061
Glycogen storage disease type 1, molecular diagnostics, special case
J0071
Hyperglycinemia, nonketotic, molecular diagnostics, special case
J0081
Hyperoxaluria, primary, type 1, molecular diagnostics, special case
J0091
Isovalericacidemia, molecular diagnostics, special case
J0101
Lipoamide Dehydrogenase Deficiency, molecular diagnostics, special case
J0111
Maple syrup urine disease, molecular diagnostics, special case
J0121
Methylmalonicaciduria, mutase deficiency, molecular diagnostics, special case
J0131
Molybdenum cofactor deficiency, molecular diagnostics, special case
J0141
Peroxysomal disorders, molecular diagnostics, special case
J0151
Phenylketonuria, molecular diagnostics, special case
J0161
Thiamine-responsive megaloblastic anemia, molecular diagnostics, special case
J0171
Tyrosinemia, molecular diagnostics, special case
J0181
VLCAD (Very Long Chain Acyl CoA Dehydrogenase) deficiency, molecular diagnostics, special case
J0191
Wilson disease, molecular diagnostics, special case
J0201
Xanthinuria, type I, molecular diagnostics, special case
J0211
CTX (Cerebrotendinous xanthomatosis), molecular diagnostics, special case
J0221
Hypercholesterolemia, familial, molecular diagnostics, special case
J0232
Lysosomal acid phosphatase deficiency, biochemical diagnostics
1 799,00
J0241
Aspartylglucosaminuria, molecular diagnostics, special case
J0242
Aspartylglucosaminuria, biochemical diagnostics
J0251
Ceroid lipofuscinosis, molecular diagnostics, special case
J0252
Ceroid lipofuscinosis, biochemical diagnostics
J0262
Cholesteryl ester storage disease, biochemical diagnostics
J0272
Cystinosis, nephropathic, biochemical diagnostics
J0281
Fabry disease, molecular diagnostics, special case
J0282
Fabry disease, biochemical diagnostics
J0292
Free sialic acid storage disease, biochemical diagnostics
J0302
Fucosidosis, biochemical diagnostics
J0312
GM1 gangliosidosis, biochemical diagnostics
J0322
Galactosialidosis, biochemical diagnostics
J0331
Gaucher disease, molecular diagnostics, special case
816,00
J0332
Gaucher disease, biochemical diagnostics
J0341
Glycogen storage disease type 2, Pompe, molecular diagnostics, special case
J0342
Glycogen storage disease type 2, Pompe, biochemical diagnostics
J0351
Ichthyosis, X-linked, molecular diagnostics, special case
J0352
Ichthyosis, X-linked, biochemical diagnostics
J0361
Krabbe disease, molecular diagnostics, special case
J0362
Krabbe disease, biochemical diagnostics
J0372
Mannosidosis, alpha, biochemical diagnostics
J0382
Mannosidosis, beta, biochemical diagnostics
J0392
Maroteaux-Lamy syndrome, biochemical diagnostics
J0400
Metachromatic leukodystrophy, pseudo deficiency, molecular diagnostics
J0401
Metachromatic leukodystrophy, molecular diagnostics, special case
J0402
Metachromatic leukodystrophy, biochemical diagnostics
J0412
Mucolipidosis II, biochemical diagnostics
4 091,00
J0421
Mucolipidosis III, molecular diagnostics, special case
J0422
Mucolipidosis III, biochemical diagnostics
J0431
Mucolipidosis IV, molecular diagnostics, special case
J0442
Mucopolysaccharidosis II, biochemical diagnostics
J0452
Mucopolysaccharidosis IV, biochemical diagnostics
J0462
Mucopolysaccharidosis I, biochemical diagnostics
J0472
Mucopolysaccharidosis VII, biochemical diagnostics
J0482
Multiple sulfatase deficiency, biochemical diagnostics
J0491
Niemann-Pick disease, molecular diagnostics, special case
J0492
Niemann-Pick disease, biochemical diagnostics
J0501
Niemann-Pick disease, type C, molecular diagnostics, special case
J0502
Niemann-Pick disease, type C, biochemical diagnostics
6 116,00
J0511
Pycnodysostosis, molecular diagnostics, special case
J0512
Pycnodysostosis, biochemical diagnostics
J0522
Salla disease, biochemical diagnostics
J0532
Sanfilippo syndrome, biochemical diagnostics
J0542
Schindler disease, biochemical diagnostics
J0552
Sialidosis, biochemical diagnostics
J0561
Tay Sachs, molecular diagnostics, special case
J0562
Tay Sachs, biochemical diagnostics
J0572
Wolman disease, biochemical diagnostics
J0581
Mitochondrial disorder, molecular diagnostics, special case
J0582
Mitochondrial disorder, biochemical diagnostics
J0591
Deafness, mitochondrial, molecular diagnostics, special case
J0600
Kearns Sayre Syndrome, KSS, molecular diagnostics
1 494,00
J0610
Leber Optic Atrophy, LHON, molecular diagnostics
J0621
Leigh syndrome, molecular diagnostics, special case
J0622
Leigh syndrome, biochemical diagnostics
J0631
Mitochondrial myopathy, Encephalopathy, Lactic Acidosis and Stroke-like episodes, MELAS, molecular diagnostics, special case
