Enterprise HL7 / FHIR Terminology Engine
Universal Clinical Codes & Terminology Search
Search, verify, and inspect standardized LOINC, SNOMED CT, ICD-10-CM, RxNorm, and CPT clinical codes with native HL7 FHIR R4 resource mappings.
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| Code Value | Display Description | Code System & OID | FHIR Resource | Category | Status | Actions |
|---|---|---|---|---|---|---|
|
1003449005
|
Paternal 14q32.2 microdeletion (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100345008
|
DEXTROSE 5% IN 1/2 STRENGTH SALINE
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003460001
|
Progressive avascular necrosis of bilateral lunate bones (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100346009
|
DEXTROSE 5% IN LACTATED RINGER'S
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003461002
|
Focal cortical dysplasia type II (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003462009
|
Focal cortical dysplasia type Ib
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003463004
|
Focal cortical dysplasia type I
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003464005
|
Focal cortical dysplasia type Ia
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003465006
|
Familial spinal neurofibromatosis
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003466007
|
Fetal disorder due to maternal autoimmune disease
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003468008
|
Congenital teratoma of nasopharynx
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100347000
|
DEXTROSE 5% IN SALINE 0.9%
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003470004
|
Screening for cancer done
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003471000
|
Orthostatic Hypotension Questionnaire
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003472007
|
Referral to patient navigation service
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003473002
|
B cell lymphocyte aplasia caused by drug (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003474008
|
Oral specimen collection swab (physical object)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003475009
|
Cardiac irreversible electroporation system catheter
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003476005
|
Eye tracking brain injury assessment device (physical object)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100348005
|
DEXTROSE 50%
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
Healthcare Terminology & FHIR R4 Interoperability
Standardized coding guidelines governed by CodesForMD
In HL7 FHIR R4, discrete clinical findings and laboratory measurements are encapsulated inside
Observation resources. Diagnostic terms and problem list entries are represented within Condition resources, while surgical and therapeutic acts map to Procedure. CodesForMD adheres to official US Core and International FHIR Implementation Guides.
An OID is an internationally standardized dotted-decimal identifier (e.g.
2.16.840.1.113883.6.1 for LOINC) registered with HL7 and ISO. OIDs ensure unambiguous identification of terminology authorities when exchanging clinical messages across heterogeneous EHR, LIS, and PACS systems.
Yes. You can visit our platform's administrative ingestion and export engine or contact our team to obtain batch files of standardized codes.