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 |
|---|---|---|---|---|---|---|
|
1003917004
|
Secondary hyperplasia of lung
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003918009
|
Pfeiffer syndrome type 3 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003919001
|
Postprocedural common atrioventricular valvar stenosis
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003920007
|
Sabinas brittle hair syndrome (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100392007
|
D-L-M TABLETS
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003921006
|
Sclerocornea of bilateral corneas
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003922004
|
Rothmund Thomson syndrome type 1 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003923009
|
Rothmund Thomson syndrome type 2
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003929008
|
Proximal deletion of long arm of chromosome 11 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003930003
|
Proximal deletion of long arm of chromosome 12 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100393002
|
d-L-METHIONINE POWDER
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003931004
|
Proximal deletion of long arm of chromosome 10 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003932006
|
Proximal deletion of chromosome 21 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003933001
|
Proximal deletion of long arm of chromosome 1 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003934007
|
Proximal deletion of chromosome 14
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003935008
|
Proximal deletion of chromosome 15
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003936009
|
Primary congenital hyperplasia of lung (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003937000
|
Proximal deletion of chromosome 13 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003938005
|
Phenylketonuria due to BH4 deficiency
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003939002
|
Polydactyly of bilateral index fingers (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.