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 |
|---|---|---|---|---|---|---|
|
1003392001
|
Medial deletion of long arm of chromosome 5 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003393006
|
Medial deletion of chromosome 14
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003394000
|
Medial deletion of long arm of chromosome 2
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003395004
|
Maternal uniparental disomy of chromosome 7 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003396003
|
Medial deletion of chromosome 13
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003397007
|
Congenital atresia of intestine at multiple levels
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003398002
|
Intermediate anorectal malformation with fistula
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003399005
|
Congenital anomaly of first branchial cleft (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003400003
|
Congenital gastric heterotopia of duodenum (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100340003
|
DEXAMETH-A-VET (Horses)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
10034007
|
Formyltetrahydrofolate deformylase
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003402006
|
Maternal uniparental disomy of chromosome 15
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003403001
|
Maternal uniparental disomy of chromosome 11
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003405008
|
Maternal uniparental disomy of chromosome 14
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003406009
|
Congenital intermediate sized melanocytic naevus
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003407000
|
Marfan syndrome type 1
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003408005
|
Congenital dystrophy of cornea (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003409002
|
Maternal 15q11q13 deletion (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003410007
|
Medial duplication of long arm of chromosome 5 (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100341004
|
DEXAN IRON DEXTRAN COMPLEX
|
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.