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Tests: H

Test codes, sample requirements and turnaround times for our most requested tests.

Please use the search box below to filter this list

Test name
H. Pylori Antibodies (IgG)
H. pylori culture (biopsy)
H. pylori Culture
Haematology Profile
Haemochromatosis – HFE common mutations C282Y + H63D
Haemoglobin A1c
Haemoglobin variants (alpha and beta globin gene variants) including sickle cell – ARMS PCR, RE-PCR, alpha and beta gene sequencing
Haemoglobinopathy Screen
Haemophilia A (Severe) – Factor VIII (F8) common 1/22 intron inversion
Haemophilia A CVS Variant Analysis (Known Genotype) – F8 Intron 22 Inversion, F8 Intron 1 Inversion, Sequence analysis of known variants for F8 gene
Haemophilia A (Factor VIII deficiency)
Haemophilia B CVS Variant Analysis (Known Genotype) – Sequence analysis of known variants for F9
Haemophilia B (Factor IX deficiency)
Haemophilus ducreyi by PCR
Haemophilus Influenzae Antibodies (HIB)
Hantavirus Serology/PCR
‘Hardware’ or device
Harmony® Prenatal Test (Non-Invasive Prenatal Testing) – common aneuploidy screening from maternal blood
Hearing Loss NGS Panel – full gene sequencing
Helicobacter pylori antigen
Hemophagocytic lymphohistiocytosis, familial
Hepatitis A (IgM)
Hepatitis A Immunity (Total)
Hepatitis A RNA by PCR
Hepatitis (Acute) Screen
Hepatitis B Core Antibody – IgM
Hepatitis B Core Antibody – Total
Hepatitis B DNA (Viral load)
Hepatitis B ‘e’ Antigen and Antibody
Hepatitis B Immunity
Hepatitis B (PCR) Genotype
Hepatitis B Profile
Hepatitis B Resistant Mutation
Hepatitis B Surface Antibody
Hepatitis B Surface Antigen Quantitification
Hepatitis B Surface Antigen
Hepatitis C Antibodies
Hepatitis C Antigen (Early detection)
Hepatitis C Genotype
Hepatitis C NS3 Resistance
Hepatitis C NS5a Resistance
Hepatitis C NS5b Resistance
Hepatitis C RNA (Viral Load)
Hepatitis Delta RNA (Viral load)
Hepatitis Delta total Antibody
Hepatitis E IgG/IgM
Hepatitis E RNA (Quantitative PCR)
Hereditary Cancer NGS Panel, Comprehensive – full gene sequencing + deletions/duplications
Hereditary Colon Cancer (Lynch Syndrome) NGS Panel – full gene sequencing + deletions/duplications
Hereditary Neuropathy with Liability to Pressure Palsy – PMP22 deletion analysis
Hereditary Spastic Paraplegia NGS Panel – full gene sequencing + deletions/duplications
Hermansky-Pudlak syndrome
Herpes Simplex 1 and 2 IgG typing
Herpes Simplex I/II Antibody Profile (IgG)
Herpes Simplex I/II by PCR (Swab)
HFE gene (Haemochromatosis) – common variants C282Y + H63D
High Sensitivity Crp (hsCRP)
High Sensitivity Troponin I
High Sensitivity Troponin T
Hirschprung Disease NGS Panel – full gene sequencing with deletions and duplications
Histamine Releasing Urticaria Test
Histamine (Urine)
Histone Antibodies
Histoplasma antibodies
Histoplasma antigen (Urine)
HIV-1 Genotypic Resistance (Integrase)
HIV-1 Genotypic Resistance (RT & Protease)
HIV-1 PCR Qualitative
HIV 1 Proviral DNA
HIV-1 RNA Viral Load by PCR
HIV-1 Tropism
HIV-2 drug resistance
HIV-2 Proviral DNA
HIV-2 RNA (Quantitative or Qualitative) by PCR
HIV Screening: HIV1& 2 Abs/p24 Ag (4th Gen)
HLA Tissue Typing A
HLA Tissue Typing A/B/C/DRB1/3/4/5/DQB1 (Class I & II)
HLA Tissue Typing A/B/DRB1/3/4/5
HLA Tissue Typing A/B/DRB1/3/4/5/DQB1
HLA Tissue Typing A+B
HLA Tissue Typing A+B+C (Class I)
HLA Tissue Typing B
HLA Tissue Typing B*27 only
HLA Tissue Typing B*51 (Behcet’s Disease)
HLA Tissue Typing B*57:01 high resolution
HLA Tissue Typing C
HLA Tissue Typing Coeliac Disease – DQ2/DQ8
HLA Tissue Typing DRB1/3/4/5
HLA Tissue Typing DRB1/3/4/5/DQB1 (Class II)
HLA Tissue Typing Narcolepsy – DQB1*06:02
HMG CoA Reductase Autoantibodies
HPFH and δβthalassaemia – Gap PCR, HBB MLPA, beta and gamma globin gene sequencing
HPV (mRNA HR-HPV) (ThinPrep)
HPV Genotyping
HTLV 1& 2 Abs. (Human T Lymphotropic Virus Type I-II)
Hughes Syndrome
Human Anti-Mouse Antibodies
Human Herpes Virus 6 by quantitative PCR
Human Herpes Virus 8 (HHV8) by qualitative/quantitative PCR
Human Parvovirus B19 – Quantitative DNA PCR
Huntington Disease – HD gene repeat analysis PCR
Hyperinsulinism NGS Panel – full gene sequencing
Hyperparathyroidism – CASR sequencing
Hypodysfibrinogenemia, congenital