Genetic Conditions tested at Virtus Diagnostics

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Disease
Code
Fur Further Information
PAGET DISEASE, JUVENILE
TNFRSF11B
PELIZAEUS-MERZBACHER DISEASE
PLP1
PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY
ACOX1
PHENYLKETONURIA
PAH
PIERSON SYNDROME
LAMB2
PITUITARY DWARFISM III
HESX1
PITUITARY HORMONE DEFICIENCY, COMBINED, 3;
LHX3
PLASMINOGEN DEFICIENCY TYPE I
PLG
POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE
PKHD1
PONTOCEREBELLAR HYPOPLASIA TYPE 2A
TSEN54
PONTOCEREBELLAR HYPOPLASIA TYPE 4
TSEN54
PORPHYRIA, CONGENITAL ERYTHROPOIETIC
UROS
PRECOCIOUS PUBERTY, MALE-LIMITED
LHCGR
PRIMARY LATERAL SCLEROSIS, JUVENILE
ALS2
PROPERDIN DEFICIENCY, X-LINKED
CFP
PROPIONIC ACIDEMIA
PCCB
PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE
SCNN1A
PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS;
SRD5A2
PYCNODYSOSTOSIS
CTSK
PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY
PNPO
PYRUVATE CARBOXYLASE DEFICIENCY
PC
PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY
PDHX
PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY
PDP1
PYRUVATE KINASE DEFICIENCY OF RED CELLS
PKLR