Test List: #
For reference ranges related to any specific test, please email refranges@hslpathology.com
Please note this list may not show our full repertoire of tests. If you need further information, please call +44 (0) 20 7307 9400
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1,25 Vitamin D
Code
D3
Sample Reqs
B
Special Instructions
1p36 Deletion Syndrome – karyotype + FISH
Code
KARY, FISH
Sample Reqs
CVS / AF / H
[9]
Special Instructions
[9] Clinical history must be provided.
2-Butanone GC
Code
BUTA
Sample Reqs
RU
Special Instructions
2-Furoic Acid
Code
2FA
Sample Reqs
RU
Special Instructions
4th Generation HIV1 & 2 Abs/p24 Ag (28 days post-contact)*
Code
THIV
Sample Reqs
B Tiny™
Special Instructions
*Reactive 4th & 5th Gen HIV Results require confirmation with a follow up venous blood sample.
5 HIAA
Code
RU5H
Sample Reqs
PU [1]
Special Instructions
[1] Contact the laboratory for special sample tubes/containers/instructions.
5’ Nucleotidase
Code
5NT
Sample Reqs
B
Special Instructions
6-Thioguanine Nucleotides
Code
TGN
Sample Reqs
A A
Special Instructions
7 STI Screen by PCR
Profile details
Chlamydia trachomatis
N. Gonorrhoea
Mycoplasma genitalium
Macrolide Resistance Test (M.gen)*
Ureaplasma
Trichomonas vaginalis
Gardnerella vaginalis
Herpes Simplex I/II
All tests can be requested individually.
*included if POSITIVE M.gen is detected from the same sample.
Code
PP12
Sample Reqs
FCRU or PCR or TPV or Semen
Special Instructions
11 Deoxycorticosterone
Code
DEOX
Sample Reqs
B
Special Instructions
11 Deoxycortisol
Code
11DC
Sample Reqs
B (Frozen)
Special Instructions
16S rRNA Bacterial Gene
Code
16S
Sample Reqs
J
Special Instructions
17 Hydroxyprogesterone
Code
17OH
Sample Reqs
B
Special Instructions
18S rRNA Fungal Gene
Code
18S
Sample Reqs
J
Special Instructions
21 Hydroxylase Ab’s
Code
21HA
Sample Reqs
B (Frozen)
Special Instructions
21-Hydroxylase Deficiency (Congenital Adrenal Hyperplasia) – 8 mutations screened
Code
GENE
Sample Reqs
A
[9] [11]
Special Instructions
[9] Clinical history must be provided.
[11] Patient consent required. Consent Form can be found at the back of this guide.
22q11 & 10p14 deletion (Di George Syndrome) – BOBs (5 days) + karyotype (15 days)
Code
DGB, KARY
Sample Reqs
CVS / AF / A
H
[9]
Special Instructions
[9] Clinical history must be provided.
22q11 & 10p14 deletion (Di George Syndrome) – BOBs only
Code
DGB
Sample Reqs
CVS / AF / A
[9]
Special Instructions
[9] Clinical history must be provided.