Genetic Conditions tested at Virtus Diagnostics

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Disease
Code
Fur Further Information
N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY
NAGS
NANCE-HORAN SYNDROME
NHS
NAVAJO NEUROHEPATOPATHY
MPV17
NEMALINE MYOPATHY 2
NEB
NEPHRONOPHTHISIS 1
NPHP1
NEPHRONOPHTHISIS 2
INVS
NEPHRONOPHTHISIS 4
NPHP4
NEPHROSIS 1, CONGENITAL, FINNISH TYPE
NPHS1
NEPHROTIC SYNDROME, STEROID-RESISTANT
NPHS2
NEPHROTIC SYNDROME, TYPE 3
PLCE1
NEURAMINIDASE DEFICIENCY
NEU1
NEURODEGENERATION DUE TO CEREBRAL FOLATE TRANSPORT DEFICIENCY
FOLR1
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1, HALLERVORDEN-SPATZ
PANK2
NEURONAL CEROID LIPOFUSCINOSIS 1
PPT1
NEURONAL CEROID LIPOFUSCINOSIS 2
TPP1
NEUROPATHY, CONGENITAL HYPOMYELINATING, CMT TYPE
MPZ
NEUROPATHY, CONGENITAL HYPOMYELINATING: CHARCOT-MARIE-TOOTH DISEASE, CMT4E
EGR2
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE 3
IKBKAP
NEUTROPENIA, SEVERE CONGENITAL, AUTOSOMAL RECESSIVE 3
HAX1
NEVO SYNDROME, EDS
PLOD1
NIEMANN-PICK DISEASE, TYPE A
SMPD1
NIEMANN-PICK DISEASE, TYPE B
SMPD1
NIEMANN-PICK DISEASE, TYPE C1
NPC1
NIEMANN-PICK DISEASE, TYPE C2
NPC2
NIJMEGEN BREAKAGE SYNDROME
NBN
NORRIE DISEASE
NDP