Virtus Genetics
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Genes & Diseases - What we test for

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Disease
Code
Fur Further Information
ABCD SYNDROME
EDNRB
ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME
AAAS
ACHONDROGENESIS, TYPE 1B ACG1B
SLC26A2
ACYL-CoA DEHYDROGENASE, LONG-CHAIN, DEFICIENCY OF
ACADL
ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF
ACADM
ACYL-CoA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF
ACADVL
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY - CLASSIC (SEVERE) FORM
CYP21A2
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY - SALT-WASTING FORM
CYP21A2
ADRENOLEUKODYSTROPHY
ABCD1
ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM
PEX1
ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM
PEX26
AGAMMAGLOBULINEMIA, X-LINKED
BTK
AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY
SLC12A6
AICARDI-GOUTIERES SYNDROME 1
TREX1
AICARDI-GOUTIERES SYNDROME 2
RNASEH2B
AICARDI-GOUTIERES SYNDROME 3
RNASEH2C
AICARDI-GOUTIERES SYNDROME 4
RNASEH2A
AICARDI-GOUTIERES SYNDROME 5
SAMHD1
ALLAN-HERNDON-DUDLEY SYNDROME AHDS
SLC16A2
ALPERS DIFFUSE DEGENERATION OF CEREBRAL GRAY MATTER WITH HEPATIC CIRRHOSIS
POLG
ALPHA THALASSEMIA
HBA1
ALPHA-METHYLACETOACETIC ACIDURIA
ACAT1
ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME,NONDELETION TYPE, X-LINKED
ATRX
ALPORT SYNDROME, AUTOSOMAL RECESSIVE
COL4A3
ALPORT SYNDROME, X-LINKED
COL4A5
ALSTROM SYNDROME
ALMS1
AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL
MPL
AMISH INFANTILE EPILEPSY SYNDROME
ST3GAL5
ANAUXETIC DYSPLASIA
RMRP
ANHYDROTIC ECTODERMAL DYSPLASIA, IMMUNODEFICIENCY, OSTEOPETROSIS, LYMPHEDEMA OLEDAID
IKBKG
ANTIBODY DEFICIENCY DUE TO ICOS DEFECT
ICOS
ANTLEY-BIXLER SYNDROME
POR
ARGININOSUCCINIC ACIDURIA
ASL
AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY
DDC
ARTERIAL CALCIFICATION, GENERALISED, OF INFANCY
ENPP1
ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS, 1
VPS33B
ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS, 2
VIPAR
ARTS SYNDROME
PRPS1
ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2
NLGN4
ASPHYXIATING THORACIC DYSTROPHY 2
IFT80
ASPHYXIATING THORACIC DYSTROPHY 3
DYNC2H1
ATAXIA TELANGIECTASIA
ATM
ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA
APTX
ATELOSTEOGENESIS, TYPE 2
SLC26A2
ATYPICAL MYCOBACTERIOSIS, FAMILIAL
STAT1
ATYPICAL MYCOBACTERIOSIS, FAMILIAL, 27A
IFNGR1
ATYPICAL MYCOBACTERIOSIS, FAMILIAL, 28
IFNGR2
ATYPICAL MYCOBACTERIOSIS, FAMILIAL, 29
IL12B
ATYPICAL MYCOBACTERIOSIS, FAMILIAL, 33
IKBKG
ATYPICAL MYCOBACTERIOSIS, FAMILIAL,30
IL12RB1
AUTOIMMUNE POLYENDOCRINE SYNDROME TYPE 1
AIRE
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