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 |
|---|---|---|---|---|---|---|
|
1003430006
|
Focal cortical dysplasia type IIb
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100343001
|
DEX-A-VET
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003431005
|
Mandibuloacral dysostosis co-occurrent with type A lipodystrophy (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003432003
|
Mandibuloacral dysostosis co-occurrent with type B lipodystrophy (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003433008
|
Malrotation of small intestine
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003434002
|
Lipoma due to neurospinal dysraphism
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003435001
|
Linear basal cell nevus
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003436000
|
Linear umbilical cord disruption
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003437009
|
Leydig cell hypoplasia due to complete LH receptor inactivation
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003438004
|
Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003439007
|
Intra-abdominal vitelline remnant
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003440009
|
Submucosal laryngeal cleft
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100344007
|
DEXTROSE 2 1/2% IN 1/2 STRENGTH SALINE
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003442001
|
Bilateral humero-radio-ulnar synostosis
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003443006
|
Congenital meatal stenosis of penis
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003444000
|
Type 3 lissencephaly
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003445004
|
Lumbosacral spina bifida cystica with hydrocephalus
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003446003
|
Synostosis of bilateral humerus and ulna (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003447007
|
PLP1 null syndrome
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003448002
|
Lumbosacral spina bifida aperta
|
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.