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
LHX3
PITUITARY DWARFISM III
HESX1
PITUITARY HORMONE DEFICIENCY, COMBINED, 1
POU1F1
PITUITARY HORMONE DEFICIENCY, COMBINED, 2
PROP1
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
PROPERDIN DEFICIENCY, X-LINKED
CFP
PROPIONIC ACIDEMIA
PCCA
PROPIONIC ACIDEMIA
PCCB
PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE
SCNN1A
PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE
SCNN1B
PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE
SCNN1G
PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS
SRD5A2
PYCNODYSOSTOSIS
CTSK
PYRIDOXAMINE 5'-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