|
Mitochondrial Trifunctional Protein Deficiency |
approved
|
609015 |
|
|
|
|
Molybdenum Cofactor Deficiency Type B (MOCODB) |
approved
|
252160 |
|
|
|
|
Muckle-Wells Syndrome (MWS) |
approved
|
191900 |
|
|
|
|
Mucolipidosis type II |
approved
|
252500 |
|
|
|
|
Mucopolysaccharidosis III (MPS-III) Type A (Sanfilippo syndrome A) |
approved
|
252900 |
|
|
|
|
Mucopolysaccharidosis III (MPS-III) Type B |
approved
|
252920 |
|
|
Mucopolysaccharidosis III (MPS-III) Type C |
approved
|
252930 |
|
|
Mucopolysaccharidosis III (MPS-III) Type D |
approved
|
252940 |
|
|
Mucopolysaccharidosis IVA |
approved
|
253000 |
|
|
|
|
Mucopolysaccharidosis Type I (MPS I) |
approved
|
607014, 607015, 607016 |
|
|
|
|
Mucopolysaccharidosis Type II (Hunter Syndrome) |
approved
|
309900 |
|
|
Mucopolysaccharidosis Type IVB (MPS4B) |
approved
|
253010 |
|
|
|
|
Mucopolysaccharidosis Type VI (MPS VI) (Maroteaux-Lamy Syndrome) |
approved
|
253200 |
|
|
|
|
Mucopolysaccharidosis Type VII (MPS7) |
approved
|
253220 |
|
|
|
|
Muenke Syndrome (MNKES) |
approved
|
602849 |
|
|
Multiple acyl-CoA dehydrogenase deficiency (MADD) (also known as glutaric aciduria type II) |
approved
|
231680 |
|
|
Multiple Congenital Anomalies Hypotonia – Seizures Syndrome 1 (MCAHS1) |
approved
|
614080 |
|
|
|
|
Multiple Congenital Anomalies Hypotonia – Seizures Syndrome 2 (MCAHS2) |
approved
|
300868 |
|
|
|
|
Multiple Congenital Anomalies Hypotonia – Seizures Syndrome 3 (MCAHS3) |
approved
|
615398 |
|
|
|
|
Multiple Endocrine Neoplasia Type 2A (MEN 2A) |
approved
|
171400 |
|
|
|
