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 |
|---|---|---|---|---|---|---|
|
1003371001
|
Micromelic dwarfism Fryn type
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003372008
|
Microphthalmos due to branchio-oculo-facial syndrome
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003373003
|
Microcephaly with simplified gyral pattern
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003374009
|
Microlissencephaly
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003375005
|
Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003376006
|
Medial duplication of long arm of chromosome 9
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003377002
|
Medial duplication of short arm of chromosome 1
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003378007
|
Optic nerve hypoplasia due to endocrine deficiency
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003379004
|
Osteogenesis imperfecta type V
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003380001
|
Prader-Willi-like syndrome due to microdeletion 6q16
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100338008
|
DEXAMETHASONE TABLETS
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003381002
|
Onycho-tricho-dysplasia neutropenia syndrome
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003384005
|
Multiple congenital defects of vertebral segmentation
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003385006
|
Neurodevelopmental disorder due to maternal use of alcohol (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003387003
|
Molybdenum cofactor deficiency complementation group C
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003388008
|
X-linked oligodontia (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003389000
|
Mosaic 1q duplication
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
100339000
|
DEXAMETH-A-VET (Dogs)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003390009
|
X-linked hypodontia (disorder)
|
SNOMED CT
2.16.840.1.113883.6.96
|
General | General | Active |
|
|
1003391008
|
Medial deletion of long arm of chromosome 4 (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.