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 |
|---|---|---|---|---|---|---|
|
1003318001
|
Extension Namespace {1000258} (namespace concept)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003319009
|
Extension Namespace {1000259} (namespace concept)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003320003
|
Extension Namespace 1000260
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100332009
|
DERMCAPS LIQUID
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003322006
|
Distal deletion of short arm of chromosome 3 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003324007
|
Congenital synostosis of both tibias and fibulas
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003330007
|
Simple syndactyly of toes of first web space of bilateral feet
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100333004
|
DERMETHRIN
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003337005
|
Bilateral split foot
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003339008
|
Congenital split of bilateral hands (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100334005
|
DERMOLAR SHAMPOO
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100335006
|
DEXAMETHASONE 2.0 MG INJECTION
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003358004
|
Distal deletion of short arm of chromosome 8 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100336007
|
DEXAMETHASONE INJECTION
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003364006
|
Distal deletion of chromosome 13 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003367004
|
Molybdenum cofactor deficiency complementation group A
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003368009
|
Molybdenum cofactor deficiency complementation group B
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003369001
|
Microphthalmos due to Delleman syndrome (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003370000
|
Microphthalmos due to Fryns syndrome (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100337003
|
DEXAMETHASONE SODIUM PHOSPHATE INJECTION
|
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.