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 |
|---|---|---|---|---|---|---|
|
1003900006
|
Proximal deletion of long arm of chromosome 4 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100390004
|
DL-ALPHA TOCOPHEROL ACETATE INJECTION
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
10039002
|
^210m^Bismuth
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003901005
|
Proximal deletion of long arm of chromosome 18
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003902003
|
Proximal deletion of long arm of chromosome 2
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003903008
|
Proximal deletion of long arm of chromosome 16 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003904002
|
Proximal deletion of long arm of chromosome 17 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003905001
|
Proximal duplication of chromosome 21 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003906000
|
Proximal duplication of long arm of chromosome 1
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003907009
|
Proximal duplication of chromosome 14 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003908004
|
Proximal duplication of chromosome 15 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003909007
|
Proximal duplication of chromosome 13 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100391000
|
D-LIMONENE SHAMPOO
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003910002
|
Proximal deletion of short arm of chromosome 8 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003911003
|
Proximal deletion of short arm of chromosome 9
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003912005
|
Proximal deletion of short arm of chromosome 6
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003913000
|
Proximal deletion of short arm of chromosome 7 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003914006
|
Proximal deletion of short arm of chromosome 1
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003915007
|
Proximal deletion of short arm of chromosome 3
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003916008
|
Pfeiffer syndrome type 2 (disorder)
|
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.