| Package | us.nlm.vsac |
| Type | ValueSet |
| Id | 2.16.840.1.113883.3.526.3.1424 |
| FHIR Version | R4 |
| Source | http://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113883.3.526.3.1424/expansion |
| URL | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.526.3.1424 |
| Version | 20210214 |
| Status | active |
| Date | 2022-03-07T11:14:02-05:00 |
| Name | HereditaryCornealDystrophies |
| Title | Hereditary Corneal Dystrophies |
| Realm | us |
| Authority | hl7 |
| Purpose | (Clinical Focus: The purpose of this value set is to represent concepts of a diagnosis of hereditary corneal dystrophies.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts that represent a diagnosis of hereditary corneal dystrophies, including congenital, epithelial/juvenile, granular, lattice or macular corneal dystrophies.),(Exclusion Criteria: Excludes concepts that represent a diagnosis for 'unspecified eye.') |
No resources found
| CodeSystem | |
| sct | SNOMED CT (all versions) |
| icd-10-cm | International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM) |
| sct | SNOMED codes used in this IG |
| sct | veri |
| icd-10-cm | International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM) |
| ValueSet | |
| 2.16.840.1.113883.3.526.2.1564 | Hereditary Corneal Dystrophies |
| 2.16.840.1.113883.3.526.2.1566 | Hereditary Corneal Dystrophies |
No narrative content found in resource
FHIR