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PathOlOgics, LLC

Cairo, Egypt - Halifax, Canada

Validated Genomics-Based and Clinical-Grade Diagnosis Support Systems

  • 🚀 AI-powered provider of validated clinical-grade diagnostic systems
  • 🏆 Increase productivity, reduce liability, and maximize quality
  • 🛡️ HIPAA-compliant comprehensive medical automation

Direct Benefits

Multiply productivity with quality of senior hematopathologists in NY
Induce profitability and overcome shortage

65,000+
International Cases Served ( Malignant & Benign ) using Genomics, Flow-Cytometry, CBC, and Blood Smear

Work-Fit Solutions

Physician Request
1

Physician Request

Requests for disease diagnosis or follow-up after treatment

Test Selection Advisor assists here
Lab Processing
2

Lab Processing

Samples used for CBC with or without genomic testing

Expert Exam
3

Expert Exam

Hematopathologists examine smears and review clinical data

Automated Blood Cells Analysis assists here
Reporting
4

Reporting

Hematopathologists write the final reports

Validated Automated Diagnosis assists here

Clinically Validated Diagnostic Automation

Advanced Hematopathology Report Automation -- Seamlessly Integrated

Scientifically Proven in Nature

Published in Nature Scientific Data through rigorous validation:

  • 14,441 Genomics-Based Validated Automated Comprehensive Clinicopathologic Correlations for Myeloid Neoplasms
  • Stringent validation by 51 international professors/consultants/specialists from multiple medical centres confirmed 100% medical and clerical accuracy, referencing the WHO 5th edition and relevant esteemed publications
  • Comprehensive cases of acute myeloid leukemia (AML), myelodysplastic neoplasms (MDS), myeloproliferative neoplasms (MPN), chronic myeloid leukemia (CML), overlapping MDS/MPN, and clonal haematopoiesis (CH)
View Nature Publication

Full Agentic Workflow Integration

Seamless LIS/EHR Integration delivering immediate operational value:

FHIR EMR Plugins
HL7 LIS Connectors
API Web Extensions
REST Custom Workflows
Automatically Collect Input Data and Return Diagnostic Narratives
Fully Secure and Compliant with HIPAA Regulations
Hospitals, Reference Labs, Academic Institutions, and Clinics

Enterprise Performance

200%
Faster Diagnostics
60%
Reduced Costs
100%
Medical Accuracy
♦ Auto-Verification & Auto-Interpretation of molecular analysis by next-generation sequencing ( NGS ) and PCR, flow cytometry, blood smear findings, and Complete Blood Count ( CBC )
♦ Automated Genomics-Based Comprehensive Clinico-Pathologic Correlations
♦ Generation of Pre-Final Reports for Hematopathologist Review and Sign-off

Comprehensive Diagnostic and Prognostic Coverage

List of Diseases

  • Acute leukemia with favorable, intermediate, or adverse prognosis
  • Acute leukemic transformation of non-CML myeloid neoplasm
  • High-grade MDS with increased blasts (MDS-IB2)
  • High-grade MDS (MDS-IB2) with mutated TP53
  • MDS with biallelic TP53 inactivation (MDS-biTP53)
  • MDS with increased blasts (MDS-IB1)
  • MDS with increased blasts (MDS-IB2)
  • MDS with low blasts (MDS-LB)
  • MDS with low blasts and SF3B1 mutation (MDS-SF3B1)
  • Accelerated phase of MDS/MPN
  • Chronic Myelomonocytic Leukemia (MD-CMML-1)
  • Chronic Myelomonocytic Leukemia (MD-CMML-2)
  • Chronic Myelomonocytic Leukemia (MP-CMML-1)
  • Chronic Myelomonocytic Leukemia (MP-CMML-2)
  • MDS/MPN with impending progression to accelerated phase
  • MDS/MPN with neutrophilia (atypical CML)
  • MDS/MPN with SF3B1 mutation and thrombocytosis
  • MDS/MPN, not otherwise specified
  • Accelerated phase of MPN
  • Chronic Eosinophilic Leukemia
  • Chronic Neutrophilic Leukemia
  • Essential Thrombocythemia
  • MPN with impending progression to accelerated phase
  • MPN, not otherwise specified
  • Polycythemia vera
  • Polycythemia vera with leukocytosis
  • Polycythemia vera with superimposed iron deficiency
  • Pre-fibrotic stage of Primary Myelofibrosis
  • Primary Myelofibrosis
  • Triple negative Essential Thrombocythemia
  • Myeloid neoplasm with favorable, poor, or adverse prognosis
  • Clonal Cytopenia & Monocytosis of Undetermined Significance
  • Clonal Cytopenia of Undetermined Significance
  • Clonal Hematopoiesis of Indeterminate Potential
  • Clonal Monocytosis of Undetermined Significance
  • Secondary Anemia
  • Secondary Erythrocytosis
  • Secondary Thrombocytopenia
  • Secondary Thrombocytosis
  • Secondary Leukopenia
  • Secondary Leukocytosis
  • Secondary Neutropenia
  • Secondary Neutrophilia
  • Secondary Lymphopenia
  • Secondary Lymphocytosis
  • Secondary Monocytosis
  • Secondary Eosinophilia
  • Secondary Basophilia

List of Genomics

  • ASXL1
  • BCOR
  • CALR
  • CBFB::MYH11
  • CBL
  • CEBPA
  • CSF3R
  • DEK::NUP214
  • DNMT3A "R882"
  • DNMT3A-Others
  • ETV6
  • EZH2
  • FLT3
  • GATA2
  • IDH1
  • IDH2
  • IKZF1
  • JAK2 Exon 12
  • JAK2 "V617F"
  • JAK3
  • KIT
  • KRAS
  • MLLT3::KMT2A
  • MPL
  • NF1
  • NPM1*
  • NRAS
  • PHF6
  • PML::RARA
  • PTPN11
  • RUNX1
  • RUNX1::RUNX1T1
  • SETBP1
  • SF3B1
  • SRSF2
  • STAG2
  • TET2
  • TP53-Multi-Hit
  • TP53-Single-VAF-Less-Than-50%
  • U2AF1
  • WT1
  • ZRSR2
  • BCR::ABL1 kinase domain "D276G" mutation
  • BCR::ABL1 kinase domain "E255K" mutation
  • BCR::ABL1 kinase domain "E255V" mutation
  • BCR::ABL1 kinase domain "E279K" mutation
  • BCR::ABL1 kinase domain "E292L" mutation
  • BCR::ABL1 kinase domain "E292Q" mutation
  • BCR::ABL1 kinase domain "F317C" mutation
  • BCR::ABL1 kinase domain "F317I" mutation
  • BCR::ABL1 kinase domain "F317L" mutation
  • BCR::ABL1 kinase domain "F317R" mutation
  • BCR::ABL1 kinase domain "F317V" mutation
  • BCR::ABL1 kinase domain "F359C" mutation
  • BCR::ABL1 kinase domain "F359I" mutation
  • BCR::ABL1 kinase domain "F359L" mutation
  • BCR::ABL1 kinase domain "F486S" mutation
  • BCR::ABL1 kinase domain "G250E" mutation
  • BCR::ABL1 kinase domain "H396A" mutation
  • BCR::ABL1 kinase domain "H396P" mutation
  • BCR::ABL1 kinase domain "H396R" mutation
  • BCR::ABL1 kinase domain "L248V" mutation
  • BCR::ABL1 kinase domain "L384M" mutation
  • BCR::ABL1 kinase domain "M244V" mutation
  • BCR::ABL1 kinase domain "M351T" mutation
  • BCR::ABL1 kinase domain "Q252H" mutation
  • BCR::ABL1 kinase domain "Q252R" mutation
  • BCR::ABL1 kinase domain "T315A" mutation
  • BCR::ABL1 kinase domain "T315I" mutation
  • BCR::ABL1 kinase domain "V299L" mutation
  • BCR::ABL1 kinase domain "Y253H" mutation
  • CML with 11q23 Rearrangement
  • CML with 3q26.2 Rearrangement
  • CML with 7q Deletion
  • CML with 7q Duplication
  • CML with 7q Translocation
  • CML with Complex Abnormalities ( 3 or More Chromosomal Abnormalities )
  • CML with Extra Philadelphia Chromosome
  • CML with Isochromosome 17q
  • CML with Low Risk 2ry Chromosomal Abnormalities
  • CML with Monosomy 7
  • CML with Trisomy 17
  • CML with Trisomy 19
  • CML with Trisomy 21
  • CML with Trisomy 8

Users Feedback

Quality

Top Tier

“Achieved the quality of senior hematopathologists in NYC”

Productivity

200%

“Increased productivity in labs by up to 200%”

Diagnosis Time

2 Mins

“Reduced time for comprehensive diagnosis report from 10-20 minutes to 2 minutes”

Training & Assistance

Asset

“Assisted in training junior physicians”

Staffing & Stress

Relief

“Helped overcome shortage in the lab”

Risk Management

No Errors

“Prevented medical errors”

Profitability

Maximize

“Increased profitability and reduced costs”

Interactive Guide

How to Use

Get started with our diagnostic system

Play audio

Enter the results of CBC, smear review, genetic tests, and clinical findings to receive a comprehensive clinicopathologic correlation (including diagnosis, prognosis, and recommendations) for Hematologic neoplasms and benign diseases, offering a perfect, personalized, and prognostic assessment with the quality of specialists in Hematopathology in New York

Medical Validation

Clinically validated accuracy

Play audio

Referencing the WHO 5th edition, the International Consensus Classification of Myeloid Neoplasms and Acute Leukemias, and other esteemed publications, 40 specialists and consultants from various international medical centers rigorously validated the medical and clerical accuracy, confirming 100% alignment with final Hematopathology reports

HIPAA Compliance

Zero risk data security

Play audio

There is zero risk as no patient or user information is required. No one can differentiate whether the generated diagnosis is for real cases, training purposes, or hypothetical patients

Current Innovation -- Medical Validation In Progress

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Get in Touch

Excellence in Diagnostics Across Borders

EG

Cairo, Egypt

Headquarters 21 Al Nasr Street, Nasr City
Cairo, Egypt
Direct Line +2 0122 65 777 65
Executive Lead Ahmed Elsafty CEO
AE

Dubai, UAE

Regional Office Albady Complex Villa 7
Dubai, UAE
Direct Line +971 50 370 8466
Executive Lead Mohamed Montaser General Director
AE

Dubai, UAE

Academic Hub British University in Dubai
Dubai, UAE
Direct Line +971 56 666 5416
Technical Lead Ahmed Soliman Technical Officer
CA

Halifax, Canada

North America 656 Bedford Highway
Halifax, NS Canada
Direct Line +1 782-234-6131
Operations Lead Taher Halawa Partner & Consultant

Global Inquiries

Support Channel
Response Time Within 3 Days
Available Support Technical • Medical
Languages English • Frensh • Arabic
HIPAA Compliant Secure Communication Global Coverage