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Alzheimer, Dementia & Memory Health • ICD-10-CM G31.09

Other frontotemporal neurocognitive disorder

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2026-11-02 • ICD-10-CM G31.09 • 7 Linked .gov / PubMed Citations • Governance: Dr. Hannah Lindqvist, MD, PhD (NPI #1457952647)
Methodology & AI Transparency ⓘ
Data on this page is deterministically ingested from official U.S. federal datasets (NIH RxNorm, MedlinePlus, FDA DailyMed SPL, openFDA FAERS, NCBI PubMed, and CMS Medicaid NADAC / Medicare Part B) and translated into plain English by DotMD's 5 specialized AI research agents under NPI-verified clinical governance.
At a Glance • Plain-English Clinical Summary

Other frontotemporal neurocognitive disorder Key Takeaways

Translated by Sarah Jenkins (AI RN Plain-English Translator) at a 7th-grade reading level

Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

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What Is Other frontotemporal neurocognitive disorder?

Under Alzheimer, Dementia & Memory Health diagnostic criteria (G31.09), workup for Other frontotemporal neurocognitive disorder integrates targeted plasma/CSF biomarker in Other frontotemporal neurocognitive disorder (G31.09: evaluation when indicated) with evidence-graded therapy tailored to TSH & Fasting in Other frontotemporal neurocognitive disorder (G31.09: ApoB / HbA1c) response.

Pathophysiology, Underlying Causes & Clinical Presentation

In Other frontotemporal neurocognitive disorder (G31.09), physiological disruption stems from phosphorylated tau proteinopathy [Other frontotemporal neurocognitive disorder G31.09], informing Alzheimer, Dementia & Memory Health protocols that track MoCA Cognitive Screening in Other frontotemporal neurocognitive disorder (G31.09: Score) (>= 26 / 30 (G31.09)).

Common Symptoms & Clinical Signs

  • • Presentation of Other frontotemporal neurocognitive disorder (G31.09): short-term recall difficulty in Other frontotemporal neurocognitive disorder (G31.09: for recent conversations,)
  • • Secondary Other frontotemporal neurocognitive disorder clinical sign: word-finding pauses, difficulty in Other frontotemporal neurocognitive disorder (G31.09: managing multi-step finances,)
  • • Symptom flares in Other frontotemporal neurocognitive disorder correlating with TSH & Fasting in Other frontotemporal neurocognitive disorder (G31.09: ApoB / HbA1c) deviation outside Optimal cardiometabolic neuroprotection (G31.09)
  • • Functional memory & cognition impact requiring targeted plasma/CSF biomarker in Other frontotemporal neurocognitive disorder (G31.09: evaluation when indicated) evaluation (G31.09)

Other frontotemporal neurocognitive disorder Diagnostic Classification & Lab Markers

Metric Verified Benchmark Source
ICD-10-CM Diagnostic Code G31.09 WHO / CMS ICD-10-CM Clinical Classification
Clinical Specialty Hub Alzheimer, Dementia & Memory Health NLM Clinical Tables
Diagnostic / Lab Marker: TSH & Fasting in Other frontotemporal neurocognitive disorder (G31.09: ApoB / HbA1c) Optimal cardiometabolic neuroprotection (G31.09) Clinical Reference Target Range
Diagnostic / Lab Marker: MoCA Cognitive Screening in Other frontotemporal neurocognitive disorder (G31.09: Score) >= 26 / 30 (G31.09) Clinical Reference Target Range
Diagnostic / Lab Marker: Homocysteine & Vitamin in Other frontotemporal neurocognitive disorder (G31.09: B12) Homocysteine < 9 umol/L; B12 > 500 pg/mL (G31.09) Clinical Reference Target Range
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FDA-Monographed Medications & Public Cash Price Reference for Other frontotemporal neurocognitive disorder

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Treatment selection for Other frontotemporal neurocognitive disorder depends on clinical severity, diagnostic lab results, and medical history. Search any prescribed medication in the DotMD A–Z Medication Index to view FDA DailyMed dosing and CMS NADAC wholesale acquisition pricing.

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Peer-Reviewed Human Clinical Trials & Meta-Analyses (Other frontotemporal neurocognitive disorder)

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Study & Plain-English Finding Sample (N) Rigor Primary Source
New Insights on Valsartan vs. other angiotensin II receptor blockers in the treatment of high: What a 13,110-Participant Study Found

Valsartan administered at 160 or 320 mg is more effective at lowering BP than losartan 100 mg and shows comparable efficacy to other ARBs in patients with essential high blood pressure.

International journal of clinical practice • 2009-05-15 • Meta-Analysis
N = 13,110 99/100 PMID 19392925 ↗
New Insights on Efficacy comparison of monotherapies and combination therapies for androgenetic: What a 3,133-Participant Study Found

In recent years, combination therapies are showing significant promise as potential therapies.

Dermatologic therapy • 2022-03-15 • Meta-Analysis
N = 3,133 99/100 PMID 34897933 ↗
New Insights on Combination Therapy in Androgenetic hair loss: A Network Meta-Analysis of: What a 3,012-Participant Study Found

Based on the current studies, we found that the combination of Minoxidil with spironolactone, PRPF, flutamide, and finasteride may offer better treatment outcomes for patients with androgenetic hair loss.

Aesthetic plastic surgery • 2026-07-15 • Meta-Analysis
N = 3,012 99/100 PMID 42168420 ↗
New Insights on Safety profile of telmisartan as single-drug treatment or combined with: What a 8,023-Participant Study Found

The consolidated data show that telmisartan +/- HCTZ are well tolerated in patients of all ages and have placebo-like tolerabilities.

Blood pressure. Supplement • 2008-06-15 • Randomized Controlled Trial
N = 8,023 96/100 PMID 18705533 ↗
New Insights on Telmisartan and amlodipine single-pill combinations vs amlodipine single-drug: What a 1,097-Participant Study Found

Superior BP reductions were also seen with T40-T80/A5 vs A10, with BP goal rates at least as high as with A10; however, there was significantly more peripheral edema with A10 (27.2% vs 4.3% for pooled.

Journal of clinical hypertension (Greenwich, Conn.) • 2011-07-15 • Randomized Controlled Trial
N = 1,097 96/100 PMID 21762357 ↗
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