Helios
Methodology

Methodology

What Helios reasons from, and how much of it is settled

Helios compares your labs against reference intervals. Those intervals are the whole premise of the tool, so they are published here in full — including the ones that no clinician has signed off on. This page is generated directly from the engine's range table, so it cannot quietly fall out of date with what the software actually does.

Review coverage

105
Markers in the engine

Every biomarker Helios can evaluate, numeric and qualitative.

28
Clinician-reviewed

A licensed clinician has read and signed off on the interval.

77
Not yet clinician-reviewed

No clinician has signed these off. Most have a published source behind them; some are genuinely contested.

77 of the 105 reference ranges in Helios have not been signed off by a clinician. Of those, 47 have a citable published source but no clinical sign-off, and 30 are flagged as unsettled — contested, age-dependent, derived from other values, or with no source on record at all. We publish this because a tool that implied all 105 were settled would be lying to you. Findings that rest on an unsettled range are marked as such inside the product, not hidden.

What the three review states mean

Clinician-reviewed

A licensed clinician has read this interval and signed off on it.

Evidence-established

A published source backs this interval, but no clinician has signed it off. Not the same as reviewed.

Needs review

The interval is contested, age-dependent, derived, or has no source on record. Treat it as unsettled.

These are not shades of the same thing. "Evidence-established" means a paper or guideline supports the interval — it does not mean a doctor looked at it in the context of this tool. We keep the two separate on purpose.

Two bands per marker: standard vs optimal

Every numeric marker carries two intervals, and the difference between them matters.

Standard band
The conventional laboratory "normal" — the range that covers most of the general population. Falling outside it is what a typical lab report flags. It describes what is common, which is not the same as what is healthy: it is derived from a population that includes plenty of unwell people.
Optimal band
The tighter target used in longevity and preventive practice — where the evidence suggests risk is lowest, rather than merely where most people sit. This is the band Helios flags against, which is why it will surface things your lab report called normal.

The honest caveat: optimal bands are inherently less settled than standard ones. Many rest on observational association rather than on trials showing that moving a number produces a better outcome. Each marker below carries a direction telling you which side is the concern — higher, lower, or both extremes.

Evidence tiers on recommendations

Anything Helios suggests carries a tier describing how strong the evidence behind it actually is. Tiers are never upgraded to make a suggestion look better supported than it is.

Tier A — trials and guidelines
Backed by randomised controlled trials or established clinical guidelines. The strongest thing we can say.
Tier B — cohort and mechanistic
Backed by observational cohort studies or a plausible biological mechanism. Suggestive, not proven — these show association, and association is not causation.
Tier C — emerging and anecdotal
Early research, small studies, or practitioner experience. Included for completeness and explicitly labelled. Treat with real scepticism.

What this engine will not do

  • It does not diagnose. An out-of-range marker is an observation to discuss with a clinician, never a condition.
  • It does not prescribe. Every medication, hormone, peptide, and therapy it surfaces carries dosing ranges, an evidence tier, and a requires-licensed-clinician flag. It is information to bring to an appointment, not an instruction to follow.
  • The safety gate runs before ranking, always. Interventions blocked on safety grounds — interactions, contraindications, your stated conditions — never enter the recommendation list at all. They are set aside as withheld for safety, and you can see that they were withheld.
  • It does not invent your data. Values parsed out of an uploaded lab PDF are proposals until you confirm them. Nothing extracted by OCR or a language model is trusted automatically, and uncertain values are surfaced as uncertain rather than guessed.
  • It does not send your health data to third parties. Queries to external research databases carry only topic strings such as "testosterone replacement outcomes" — never your identity, your labs, or your symptoms.

Every reference range in the engine

All 105 markers, grouped by body system. Filter by review state to see exactly what is signed and what is not. Markers flagged needs review show the reason their interval is still contested.

Cardiovascular (9)

MarkerStandard bandOptimal bandDirectionReview state
ApoB
mg/dL
<90
<70
Higher is worseClinician-reviewed
Cholesterol/HDL ratio
ratio
<5
<3.5
Higher is worseEvidence-established

Risk rises >5 (Framingham-derived ratio).

HDL-C
mg/dL
Male40–90
Female50–90
Male50–90
Female60–90
Lower is worseClinician-reviewed
LDL-C
mg/dL
<100
<70
Higher is worseClinician-reviewed
Lp(a)
nmol/L
<125
<75
Higher is worseClinician-reviewed
Non-HDL cholesterol
mg/dL
<130
<100
Higher is worseEvidence-established

Non-HDL goals — ACC/AHA / NLA.

Total cholesterol
mg/dL
125–200
150–180
Both extremes are worseEvidence-established

Desirable <200 mg/dL — NCEP ATP-III.

Triglycerides
mg/dL
<150
<80
Higher is worseClinician-reviewed
VLDL
mg/dL
<30
<20
Higher is worseEvidence-established

Calculated VLDL ~2–30 mg/dL (derived from triglycerides).

Hematologic (20)

MarkerStandard bandOptimal bandDirectionReview state
Basophils %
%
<2
<1
Higher is worseEvidence-established

WBC differential reference intervals (reference labs).

Basophils (abs)
x10^3/uL
<0.2
<0.1
Higher is worseEvidence-established

Absolute basophil count reference interval (reference labs).

Eosinophils %
%
<5
<3
Higher is worseEvidence-established

WBC differential reference intervals (reference labs).

Eosinophils (abs)
x10^3/uL
<0.5
<0.3
Higher is worseEvidence-established

Absolute eosinophil count reference interval (reference labs).

Hematocrit
%
Male38.3–50
Female35.5–44.9
Male40–48
Female37–44
Both extremes are worseClinician-reviewed
Hemoglobin
g/dL
Male13.5–17.5
Female12–15.5
Male14–16.5
Female12.5–14.5
Both extremes are worseEvidence-established

WHO anemia cutoffs M<13 / F<12 g/dL; reference labs.

Lymphocytes %
%
20–45
25–40
Both extremes are worseEvidence-established

WBC differential reference intervals (reference labs).

Lymphocytes (abs)
x10^3/uL
1–3.5
1.4–3
Both extremes are worseEvidence-established

Absolute lymphocyte count reference interval (reference labs).

MCH
pg
27–33
28–32
Both extremes are worseEvidence-established

Reference-lab adult interval ~27–33 pg.

MCHC
g/dL
32–36
33–35
Both extremes are worseEvidence-established

Reference-lab adult interval ~32–36 g/dL.

MCV
fL
80–100
85–92
Both extremes are worseEvidence-established

Reference-lab adult interval ~80–100 fL.

Monocytes %
%
2–10
3–8
Both extremes are worseEvidence-established

WBC differential reference intervals (reference labs).

Monocytes (abs)
x10^3/uL
0.1–0.9
0.2–0.7
Both extremes are worseEvidence-established

Absolute monocyte count reference interval (reference labs).

Neutrophils %
%
40–75
45–65
Both extremes are worseEvidence-established

WBC differential reference intervals (reference labs).

Neutrophils (abs)
x10^3/uL
1.8–7.5
2–6
Both extremes are worseEvidence-established

Absolute neutrophil count reference interval (reference labs).

PSA
ng/mL
<6.5age-stratified
<3
Higher is worseClinician-reviewed
Platelets
x10^3/uL
150–400
200–350
Both extremes are worseEvidence-established

Reference-lab adult interval ~150–400 x10^3/uL.

RBC
x10^6/uL
Male4.5–5.9
Female4–5.2
Male4.7–5.5
Female4.2–4.9
Both extremes are worseEvidence-established

Reference-lab adult intervals (StatPearls NBK604207).

RDW
%
<14.5
<13
Higher is worseEvidence-established

~11.5–15%; high RDW associates with mortality (PMC5640961).

WBC
x10^3/uL
3.5–10.5
4–8
Both extremes are worseEvidence-established

Reference-lab adult interval ~4.5–11.0 x10^3/uL.

Hormonal (6)

MarkerStandard bandOptimal bandDirectionReview state
DHEA-S
ug/dL
Male40–290age-stratified
Female15–160age-stratified
Male120–250
Female70–150
Lower is worseClinician-reviewed
Estradiol
pg/mL
Male10–40
Female30–400
Male20–30
Female50–200
Both extremes are worseClinician-reviewed
Free testosterone
pg/mL
Male50–200
Female1–8.5
Male120–200
Female3–7
Lower is worseClinician-reviewed
IGF-1
ng/mL
65–220age-stratified
100–180
Both extremes are worseClinician-reviewed
SHBG
nmol/L
20–60
25–45
Both extremes are worseClinician-reviewed
Total testosterone
ng/dL
Male300–1000
Female15–70
Male600–900
Female30–60
Lower is worseClinician-reviewed

Inflammation (9)

MarkerStandard bandOptimal bandDirectionReview state
ALT
U/L
Male<44
Female<32
Male<25
Female<20
Higher is worseEvidence-established

Healthy ULN ~29–33 (M) / 19–25 (F) U/L — ACG 2017 (PubMed 27995906).

AST
U/L
Male<40
Female<32
Male<25
Female<22
Higher is worseEvidence-established

Lab ULN ~35–40 U/L (Mayo Proceedings LFT review).

Alkaline phosphatase
U/L
40–129
50–95
Both extremes are worseEvidence-established

~30–120 U/L — Cleveland Clinic LFT.

Bilirubin (total)
mg/dL
0.2–1.2
0.3–1
Both extremes are worseNeeds review

'Lower is better' optimal is likely inverted — higher bilirubin associates with antioxidant/protective effects. See docs/RANGE_EVIDENCE.md (fix #6).

ESR
mm/hr
Male<20
Female<30
Male<10
Female<15
Higher is worseNeeds review

Age-dependent (Westergren; Miller upper bound ≈ age/2). Our fixed band is wide and not age-adjusted — no authoritative endorsement. See docs/RANGE_EVIDENCE.md §C.

GGT
U/L
Male<65
Female<45
Male<20
Female<16
Higher is worseClinician-reviewed
Homocysteine
umol/L
<15
<8
Higher is worseClinician-reviewed
Rheumatoid factor
IU/mL
<14
<10
Higher is worseEvidence-established

Normal <14(–20) IU/mL — Cleveland Clinic.

hs-CRP
mg/L
<3
<1
Higher is worseClinician-reviewed

Metabolic (15)

MarkerStandard bandOptimal bandDirectionReview state
Albumin
g/dL
3.5–5
4.3–5
Both extremes are worseEvidence-established

3.5–5.0 g/dL — Medscape lab values.

Albumin/Globulin ratio
ratio
1–2.5
1.2–2.2
Both extremes are worseNeeds review

Derived albumin/globulin ratio; no authoritative optimal interval. See docs/RANGE_EVIDENCE.md.

Bicarbonate (CO2)
mmol/L
22–30
24–28
Both extremes are worseEvidence-established

22–29 mmol/L — Mayo BMP reference.

Calcium
mg/dL
8.6–10.3
9.2–10
Both extremes are worseEvidence-established

8.4–10.6 mg/dL — Medscape lab values.

Chloride
mmol/L
98–107
100–106
Both extremes are worseEvidence-established

98–107 mmol/L — Mayo reference.

Fasting glucose
mg/dL
70–99
75–90
Higher is worseClinician-reviewed
Fasting insulin
uIU/mL
2–19
2–6
Higher is worseClinician-reviewed
Globulin
g/dL
2–3.9
2.4–3.2
Both extremes are worseNeeds review

Calculated (total protein − albumin); upper bound wide with no authoritative optimal interval. See docs/RANGE_EVIDENCE.md.

HOMA-IR
index
<2.5
<1.5
Higher is worseClinician-reviewed
HbA1c
%
4–5.6
4.5–5.3
Both extremes are worseClinician-reviewed
Phosphate
mg/dL
2.5–4.5
3–4
Both extremes are worseEvidence-established

2.5–4.5 mg/dL — Medscape lab values.

Potassium
mmol/L
3.5–5.1
4–4.8
Both extremes are worseEvidence-established

3.6–5.2 mmol/L — Mayo reference.

Sodium
mmol/L
135–145
137–142
Both extremes are worseEvidence-established

135–145 mmol/L — Mayo BMP reference.

Total protein
g/dL
6–8.3
6.5–7.8
Both extremes are worseEvidence-established

6.3–8.3 g/dL — Medscape lab values.

Uric acid
mg/dL
Male3.4–7
Female2.4–6
Male3.5–5.5
Female3–5
Both extremes are worseEvidence-established

Reference intervals; treat-to-target <6.0 mg/dL — ACR 2020 gout (PubMed 32391934).

Micronutrient (23)

MarkerStandard bandOptimal bandDirectionReview state
Ceruloplasmin
mg/dL
20–35
20–35
Both extremes are worseNeeds review

Acute-phase reactant; primarily interpreted alongside copper rather than alone. Reviewer must confirm it warrants a standalone finding at all. Worksheet Q2. D8 2026-08-21: the independent review (docs/OPEN_CLINICAL_QUESTIONS_INDEPENDENT_REVIEW.md) refused the 22–32 optimal band; demoted to the standard interval. Its stronger ask — no standalone finding, only a combined copper/ceruloplasmin one — is specialist residue (the combined finding adds a claim).

~20–35 mg/dL adult reference interval (reference labs).

Copper
ug/dL
70–140
70–140
Both extremes are worseNeeds review

Rises as an acute-phase reactant via ceruloplasmin, so an elevated value may be inflammation, not copper excess. Reviewer must rule on the optimal band and the inflammation caveat. Worksheet Q2. D8 2026-08-21: the independent review (docs/OPEN_CLINICAL_QUESTIONS_INDEPENDENT_REVIEW.md) refused the 85–130 optimal band; demoted to the laboratory interval.

~70–140 µg/dL adult serum reference interval (reference labs; NIH ODS).

Ferritin
ng/mL
Male30–400
Female15–200
Male50–150
Female40–120
Both extremes are worseClinician-reviewed
Folate
ng/mL
3–20
10–20
Lower is worseEvidence-established

Deficiency <3–4 ng/mL (NHANES-derived).

Iron
ug/dL
Male65–175
Female50–170
Male90–150
Female70–140
Both extremes are worseEvidence-established

~50–175 µg/dL adult reference (Medscape).

Magnesium (serum)
mg/dL
1.7–2.2
2–2.2
Both extremes are worseNeeds review

Serum magnesium is a poor whole-body-status marker: roughly 1% of body magnesium is extracellular and the serum level is tightly defended, so a normal value does not exclude depletion. Reviewer must rule on the optimal band, and on whether serum magnesium should classify at all when RBC magnesium is available. No worksheet entry yet — needs one.

Serum magnesium ~1.7–2.2 mg/dL adult reference interval (reference labs; NIH ODS) — distinct from RBC magnesium.

Manganese
ug/L
0.4–1.6
0.6–1.4
Both extremes are worseNeeds review

Serum and whole-blood intervals differ by an order of magnitude and the lab record carries no specimen type, so the marker is context-gated (never auto-flagged) rather than risk reading a whole-blood value as toxicity. Reviewer must rule on whether to classify it at all, and on which specimen. No worksheet entry yet — needs one.

Serum/plasma ~0.4–1.6 µg/L; WHOLE BLOOD ~4–15 µg/L — specimen-dependent and not interchangeable (reference labs).

Methylmalonic acid (MMA)
umol/L
<0.4
<0.27
Higher is worseNeeds review

Renally cleared — impaired eGFR raises it independently of B12 status. Reviewer must rule on the optimal ceiling and whether to gate on eGFR. Worksheet Q6. D8 2026-08-21: per the independent review (docs/OPEN_CLINICAL_QUESTIONS_INDEPENDENT_REVIEW.md), ≤0.27 µmol/L stays only as a contextual decision point: below eGFR 60 no MMA-alone classification; eGFR 60–89 or age ≥70 annotates reduced specificity; with a serum B12 on file the finding is framed as possible functional B12 deficiency requiring renal and clinical context.

Serum methylmalonic acid normal ≲0.40 µmol/L; elevation supports functional B12 deficiency (reference labs).

Omega-3 Index
%
4–12
8–12
Lower is worseNeeds review

Optimal >=8% derives from a specific standardized RBC assay; values from other assays are not interchangeable. Reviewer must rule on whether to flag at all when the assay is unknown. Worksheet Q8. D8 2026-08-21: the independent review (docs/OPEN_CLINICAL_QUESTIONS_INDEPENDENT_REVIEW.md) ruled an unknown assay UNCLASSIFIED, not caveated — the engine holds no assay metadata, so the marker is context-gated (stored, displayed, no automated finding). Classification returns when assay provenance can be verified.

RBC EPA+DHA; <4% high risk, 4–8% intermediate, ≥8% desirable (Omega-3 Index, Harris & von Schacky) — assay-specific.

RBC Magnesium
mg/dL
4–6.4
5–6.4
Lower is worseClinician-reviewed
RBC folate
ng/mL
140–800
140–800
Lower is worseNeeds review

Deficiency cutoffs are established; the OPTIMAL band is not, and the neural-tube-prevention threshold is a different question from adult optimization. Reviewer must rule on the optimal band. Worksheet Q6. D8 2026-08-21: the independent review (docs/OPEN_CLINICAL_QUESTIONS_INDEPENDENT_REVIEW.md) refused the 400–800 general-adult band; general adults use the deficiency limit (<140 ng/mL) only. The WHO >400 ng/mL population-level NTD-prevention target for people capable of pregnancy is specialist residue — the profile may not carry the needed field and implementing it adds a claim.

Deficiency <140 ng/mL; adult interval ~140–800 ng/mL (NHANES-derived).

Selenium
ug/L
70–150
70–150
Both extremes are worseNeeds review

Narrow therapeutic width and strongly geography/soil-dependent — a band defensible in one population may not be in another. Reviewer must rule on the optimal band and the toxicity ceiling. Worksheet Q3. D8 2026-08-21: the independent review (docs/OPEN_CLINICAL_QUESTIONS_INDEPENDENT_REVIEW.md) refused the 100–150 optimal band; demoted. High-side values below the 400 µg/L selenosis-association referral are framed as exposure review, not toxicity.

~70–150 µg/L adult serum/plasma reference interval (reference labs; NIH ODS).

TIBC
ug/dL
250–450
250–400
Both extremes are worseEvidence-established

~250–370(–450) µg/dL (Medscape).

Transferrin saturation
%
20–50
25–40
Both extremes are worseEvidence-established

20–50% (<20 deficient, >50 overload) — Medscape.

Urinary iodine
ug/L
100–299
100–199
Both extremes are worseNeeds review

WHO cutoffs are POPULATION medians from spot samples; within-person day-to-day variation is very large, so one value cannot classify an individual. Context-gated (never auto-flagged). Worksheet Q7.

WHO adequacy 100–199 µg/L as a POPULATION median from spot urine (WHO/UNICEF/ICCIDD) — not an individual diagnostic.

Vitamin A (retinol)
ug/dL
30–65
30–65
Both extremes are worseNeeds review

Serum retinol is homeostatically defended until liver stores are depleted, so it detects deficiency late. Reviewer must rule on the optimal band and the toxicity ceiling. Worksheet Q4. D8 2026-08-21: the independent review (docs/OPEN_CLINICAL_QUESTIONS_INDEPENDENT_REVIEW.md) refused the 40–60 optimal band and any serum-retinol toxicity ceiling as a diagnosis; demoted to the lab interval. The ~100 µg/dL referral trigger in micronutrient_excess is retained DELIBERATELY as the residue the licensed specialists rule on — it frames a referral, not a toxicity diagnosis.

Serum retinol ~30–65 µg/dL adult reference interval (reference labs; NIH ODS).

Vitamin B12
pg/mL
200–900
500–900
Lower is worseClinician-reviewed
Vitamin B6 (PLP)
nmol/L
20–125
30–110
Both extremes are worseNeeds review

The high side is the unsettled part: supplemental-B6 sensory neuropathy is well described but the plasma-PLP threshold at which to warn is not agreed, and assays differ. Reviewer must rule on the optimal band and on the toxicity ceiling. No worksheet entry yet — needs one.

Plasma pyridoxal 5'-phosphate ~20–125 nmol/L; deficiency commonly cited below 20–30 nmol/L (NHANES-derived; NIH ODS).

Vitamin C (ascorbate)
mg/dL
0.4–2
0.8–2
Lower is worseNeeds review

Plasma ascorbate reflects recent intake rather than tissue stores and falls with smoking and acute inflammation. Deficiency cutoffs are established; the OPTIMAL band is not. Reviewer must rule on the optimal band. No worksheet entry yet — needs one.

Plasma ascorbic acid: deficiency <0.2 mg/dL, marginal 0.2–0.4 mg/dL, adequate ≳0.4 mg/dL (NHANES-derived; NIH ODS).

Vitamin D (25-OH)
ng/mL
30–100
50–80
Both extremes are worseClinician-reviewed
Vitamin E (alpha-tocopherol)
mg/L
5.5–17
5.5–17
Both extremes are worseNeeds review

Interpretation is lipid-dependent (alpha-tocopherol:lipid ratio). Marked requires_context so no automated finding fires until that ratio is collected. Reviewer must rule on whether to keep it context-gated. Worksheet Q4. D8 2026-08-21: the independent review (docs/OPEN_CLINICAL_QUESTIONS_INDEPENDENT_REVIEW.md) refused the 10–17 optimal band; demoted. The validated lipid-standardized deficiency threshold (≈0.8 mg/g total lipids) is specialist residue.

Serum alpha-tocopherol ~5.5–17 mg/L adult reference interval (reference labs).

Vitamin K (phylloquinone)
ng/mL
0.1–2.2
0.1–2.2
Both extremes are worseNeeds review

NO defensible individual reference interval — serum phylloquinone is a poor status marker and assays are unstandardized. Context-gated (never auto-flagged). Reviewer must rule on whether to record it at all. Worksheet Q5.

No standardized individual interval; serum phylloquinone assays vary widely — recorded, not classified.

Zinc
ug/dL
70–120
70–120
Both extremes are worseNeeds review

Serum/plasma zinc is a weak status marker (homeostatically defended, falls with inflammation and albumin). Reviewer must rule on the optimal band AND whether to require joint interpretation with copper. Worksheet Q1. D8 2026-08-21: the independent review (docs/OPEN_CLINICAL_QUESTIONS_INDEPENDENT_REVIEW.md) refused the 90–120 optimal band; demoted to the standard interval pending the specialist ruling on condition-specific decision limits.

~70–120 µg/dL adult serum/plasma reference interval (reference labs; NIH ODS).

Oncologic-Screening (4)

MarkerStandard bandOptimal bandDirectionReview state
AFP
ng/mL
<8
<5
Higher is worseEvidence-established

Adult reference <8 ng/mL (lab-variable).

CA 125
U/mL
<35
<30
Higher is worseEvidence-established

Standard cutoff <35 U/mL.

CA 19-9
U/mL
<37
<30
Higher is worseEvidence-established

Standard manufacturer cutoff <37 U/mL.

CEA
ng/mL
<3
<2.5
Higher is worseEvidence-established

Nonsmoker <3.0 ng/mL — Cleveland Clinic.

Renal (15)

MarkerStandard bandOptimal bandDirectionReview state
BUN
mg/dL
7–20
10–18
Both extremes are worseEvidence-established

6–21 mg/dL — Medscape lab values.

Creatinine
mg/dL
Male0.7–1.3
Female0.6–1.1
Male0.8–1.1
Female0.6–1
Both extremes are worseEvidence-established

M 0.74–1.35 / F 0.59–1.04 mg/dL — Medscape lab values.

Urine RBC
qualitative
Qualitative (present / absent) — no numeric bandBoth extremes are worseNeeds review

No source on record for this interval.

Urine WBC
qualitative
Qualitative (present / absent) — no numeric bandBoth extremes are worseNeeds review

No source on record for this interval.

Urine bilirubin
qualitative
Qualitative (present / absent) — no numeric bandBoth extremes are worseNeeds review

No source on record for this interval.

Urine blood
qualitative
Qualitative (present / absent) — no numeric bandBoth extremes are worseNeeds review

No source on record for this interval.

Urine glucose
qualitative
Qualitative (present / absent) — no numeric bandBoth extremes are worseNeeds review

No source on record for this interval.

Urine ketones
qualitative
Qualitative (present / absent) — no numeric bandBoth extremes are worseNeeds review

No source on record for this interval.

Urine leukocyte esterase
qualitative
Qualitative (present / absent) — no numeric bandBoth extremes are worseNeeds review

No source on record for this interval.

Urine nitrite
qualitative
Qualitative (present / absent) — no numeric bandBoth extremes are worseNeeds review

No source on record for this interval.

Urine pH
pH
4.5–8
6–7
Both extremes are worseEvidence-established

4.5–8.0 — AAFP urinalysis.

Urine protein
qualitative
Qualitative (present / absent) — no numeric bandBoth extremes are worseNeeds review

No source on record for this interval.

Urine specific gravity
SG
1.005–1.03
1.01–1.025
Both extremes are worseEvidence-established

1.005–1.030 — Cleveland Clinic.

Urine urobilinogen
qualitative
Qualitative (present / absent) — no numeric bandBoth extremes are worseNeeds review

No source on record for this interval.

eGFR
mL/min/1.73m2
45–120age-stratified
60–120
Lower is worseClinician-reviewed

Serology (1)

MarkerStandard bandOptimal bandDirectionReview state
HIV 1/2 antibody
qualitative
Qualitative (present / absent) — no numeric bandBoth extremes are worseNeeds review

No source on record for this interval.

Thyroid (3)

MarkerStandard bandOptimal bandDirectionReview state
Free T3
pg/mL
2.3–4.2
3.2–4.2
Lower is worseClinician-reviewed
Free T4
ng/dL
0.8–1.8
1.1–1.6
Both extremes are worseClinician-reviewed
TSH
mIU/L
0.4–4.5
0.8–2
Both extremes are worseClinician-reviewed

Generated from packages/engine/helios/reference_ranges.py. The published figures are recomputed from the engine's range table rather than maintained by hand, and a test in the engine suite fails if this page falls behind the code.