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 |
|---|---|---|---|---|---|---|
|
1003411006
|
Medial duplication of long arm of chromosome 7 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003412004
|
Medial duplication of long arm of chromosome 2
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003413009
|
Medial duplication of long arm of chromosome 4 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003414003
|
Medial duplication of chromosome 14 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003415002
|
Medial duplication of long arm of chromosome 1
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003416001
|
Medial duplication of chromosome 13 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003417005
|
Medial deletion of short arm of chromosome 1
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003418000
|
Medial deletion of long arm of chromosome 1
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003419008
|
Medial deletion of long arm of chromosome 7 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003420002
|
Medial deletion of long arm of chromosome 9 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100342006
|
DEXASONE
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003421003
|
Intra-abdominal omphalomesenteric duct cyst (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003422005
|
Hypoplasia of optic nerve due to central nervous system malformation
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003423000
|
Dislocation of incudostapedial articulation
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003424006
|
Hutterite type cataract (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003425007
|
Glaucoma due to Lowe syndrome
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003426008
|
Glomerular disease due to Fabry disease
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003427004
|
Genochondromatosis type 1 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003428009
|
Glaucoma due to congenital anomaly of eye
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003429001
|
Focal cortical dysplasia type IIa
|
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.