Genetic Conditions tested at Virtus Diagnostics

1 | 3 | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | R | S | T | U | V | W | X | Z
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, AUTOSOMAL RECESSIVE
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
NEURONAL CEROID LIPOFUSCINOSIS 3
CLN3
NEURONAL CEROID LIPOFUSCINOSIS 5
CLN5
NEUROPATHY, CONGENITAL HYPOMYELINATING: CHARCOT-MARIE-TOOTH DISEASE, TYPE
EGR2
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III
IKBKAP
NEUTROPENIA, SEVERE CONGENITAL, AUTOSOMAL RECESSIVE 3
HAX1
NEVO SYNDROME EDS
PLOD1
NIEMANN-PICK DISEASE, TYPE
NPC2
NIEMANN-PICK DISEASE, TYPE A
SMPD1
NIEMANN-PICK DISEASE, TYPE B
SMPD1
NIEMANN-PICK DISEASE, TYPE C1
NPC1
NIJMEGEN BREAKAGE SYNDROME
NBN
NORRIE DISEASE
NDP