Genetic Conditions tested at Virtus Diagnostics

MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY

MANNOSIDOSIS, ALPHA B, LYSOSOMAL

MAPLE SYRUP URINE DISEASE TYPE 1A

MAPLE SYRUP URINE DISEASE TYPE 1B, BRANCHED-CHAIN KETO ACID DEHYDROGENASE E1, BETA POLYPEPTIDE

MAPLE SYRUP URINE DISEASE TYPE 2

MARINESCO-SJOGREN SYNDROME

MARTSOLF SYNDROME

MASA SYNDROME

MECKEL SYNDROME TYPE 1

MECKEL SYNDROME, TYPE 5

MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS

MENKES DISEASE

MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA

MENTAL RETARDATION AUTOSOMAL RECESSIVE 6

MENTAL RETARDATION WITH CEREBELLAR HYPOPLASIA & DISTINCTIVE FACIAL APPEARANCE

MENTAL RETARDATION X-LINKED 19 INCLUDED

MENTAL RETARDATION X-LINKED 72

MENTAL RETARDATION X-LINKED 88

MENTAL RETARDATION X-LINKED 90

MENTAL RETARDATION X-LINKED ASSOCIATED WITH FRAGILE SITE

MENTAL RETARDATION X-LINKED SYP-RELATED, 96

MENTAL RETARDATION X-LINKED WITH BRACHYDACTYLY AND MACROGLOSSIA

MENTAL RETARDATION, 12

MENTAL RETARDATION, 13

MENTAL RETARDATION, 7

MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1

MENTAL RETARDATION, AUTOSOMAL, 5

MENTAL RETARDATION, SYNDROMIC, 35

MENTAL RETARDATION, X-LINKED

MENTAL RETARDATION, X-LINKED 21

MENTAL RETARDATION, X-LINKED 30

MENTAL RETARDATION, X-LINKED 41,48 MRX41,48

MENTAL RETARDATION, X-LINKED 46

MENTAL RETARDATION, X-LINKED 59

MENTAL RETARDATION, X-LINKED 9

MENTAL RETARDATION, X-LINKED 93

MENTAL RETARDATION, X-LINKED ANGELMAN, SYNDROMIC, CHRISTIANSON

MENTAL RETARDATION, X-LINKED, 63

MENTAL RETARDATION, X-LINKED, 89

MENTAL RETARDATION, X-LINKED, 92

MENTAL RETARDATION, X-LINKED, 97

MENTAL RETARDATION, X-LINKED, SNYDER-ROBINSON TYPE

MENTAL RETARDATION, X-LINKED, SYNDROMIC

MENTAL RETARDATION, X-LINKED, SYNDROMIC 10

MENTAL RETARDATION, X-LINKED, SYNDROMIC, 14

MENTAL RETARDATION, X-LINKED, SYNDROMIC, 30

MENTAL RETARDATION, X-LINKED, SYNDROMIC, 9

MENTAL RETARDATION, X-LINKED, SYNDROMIC, TURNER TYPE

MENTAL RETARDATION, X-LINKED, WITH PANHYPOPITUITARISM

METACHROMATIC LEUKODYSTROPHY

METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY

METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE

METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-CoA MUTASE DEFICIENCY

METHYLMALONIC ACIDURIA, cblA TYPE

METHYLMALONIC ACIDURIA, cblB TYPE

MEVALONIC ACIDURIA

MICROPHTHALMIA, SYNDROMIC 2

MICROPHTHALMIA, SYNDROMIC 9, MATTHEW-WOOD SYNDROME

MITOCHONDRIAL COMPLEX III DEFICIENCY

MITOCHONDRIAL COMPLEX III DEFICIENCY

MITOCHONDRIAL COMPLEX III DEFICIENCY, TYPE 1

MITOCHONDRIAL DNA DEPLETION SYNDROME, HEPATOCEREBRAL FORM

MITOCHONDRIAL DNA DEPLETION SYNDROME, HEPATOCEREBRAL FORM

MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME

MOLYBDENUM COFACTOR DEFICIENCY

MOLYBDENUM COFACTOR DEFICIENCY A

mtDNA DEPLETION, ENCEPHALOMYOPATHIC FORM

mtDNA DEPLETION, ENCEPHALOMYOPATHIC FORM, 5

mtDNA DEPLETION, HEPATOCEREBRAL FORM

mtDNA DEPLETION, LACTIC ACIDOSIS, FATAL INFANTILE, 9

mtDNA DEPLETION, MYOPATHIC FORM

MUCOLIPIDOSIS II ALPHA/BETA

MUCOLIPIDOSIS III ALPHA/BETA

MUCOLIPIDOSIS IV

MUCOPOLYSACCHARIDOSIS TYPE 3A (Sanfilippo type A)

MUCOPOLYSACCHARIDOSIS TYPE 7, SLY SYNDROME

MUCOPOLYSACCHARIDOSIS TYPE II

MUCOPOLYSACCHARIDOSIS TYPE IIIC (Sanfilippo type c)

MUCOPOLYSACCHARIDOSIS TYPE VI MAROTEAUX-LAMY

MULIBREY NANISM

MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCY

MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCY

MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCY

MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT

MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE

MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE

MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE

MUSCLE-EYE-BRAIN DISEASE

MUSCLE-EYE-BRAIN DISEASE

MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A

MUSCULAR DYSTROPHY, CONGENITAL, 1C

MUSCULAR DYSTROPHY, CONGENITAL, TYPE 1D

MUSCULAR DYSTROPHY, DUCHENNE TYPE

MYD88 DEFICIENCY

MYOCLONIC EPILEPSY OF LAFORA

MYOCLONIC EPILEPSY OF LAFORA

MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG

MYOTUBULAR MYOPATHY 1