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FHIR Server FHIR Server 3.7.4-SNAPSHOT
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FHIR Version n/a
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FHIR
© HL7.org
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Server Home |
FHIR Server FHIR Server 3.7.4-SNAPSHOT
|
FHIR Version n/a
User: [n/a]
Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 79226018 | HNSHA due to NADH diaphorase deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 2620815012 | Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH) diaphorase deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2620816013 | Hereditary nonspherocytic hemolytic anemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH) diaphorase deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2913242015 | Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2913595016 | Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3780604010 | Hereditary nonspherocytic haemolytic anaemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 79226018 | HNSHA due to NADH diaphorase deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 784994016 | HNSHA due to NADH diaphorase deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 784994016 | HNSHA due to NADH diaphorase deficiency (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 2612396011 | Hereditary nonspherocytic hemolytic anemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH) diaphorase deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2620815012 | Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH) diaphorase deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2620816013 | Hereditary nonspherocytic hemolytic anemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH) diaphorase deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2913242015 | Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2913242015 | Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2913595016 | Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2913595016 | Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3780604010 | Hereditary nonspherocytic haemolytic anaemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 6300041000241119 | anémie hémolytique héréditaire non sphérocytaire due à un déficit en nicotinamide adénine dinucléotide diaphorase réduit | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 6300051000241116 | anémie hémolytique héréditaire non sphérocytaire due à un déficit en NADH (nicotinamide adenine dinucleotide hydrogen) diaphorase réduit | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 6300041000241119 | anémie hémolytique héréditaire non sphérocytaire due à un déficit en nicotinamide adénine dinucléotide diaphorase réduit | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 6300051000241116 | anémie hémolytique héréditaire non sphérocytaire due à un déficit en NADH (nicotinamide adenine dinucleotide hydrogen) diaphorase réduit | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Is a | Hereditary disorder of haematologic sysem | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Is a | Erythrocyte enzyme deficiency | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Is a | Congenital anomaly of the haematopoietic system | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Is a | Anemia due to enzyme deficiency | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Is a | Inborn error of metabolism | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Finding site | Erythrocyte | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 4 | |
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Finding site | Hematopoietic system structure | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 5 | |
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Is a | Hereditary nonspherocytic haemolytic anaemia | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Associated etiologic finding | Enzymopathy | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Finding site | Hematopoietic system structure | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Has definitional manifestation | érythropénie | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Due to | Enzymopathy | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 6 | |
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Is a | Congenital anemia | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Has definitional manifestation | Hemolysis | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Has interpretation | Below reference range | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Interprets | Red blood cell count | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Has interpretation | Below reference range | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 2 | |
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Interprets | Measurement of total haemoglobin concentration | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 2 | |
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Interprets | Erythrocyte destruction | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Has interpretation | Present (qualifier value) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 3 | |
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) | Interprets | Haemolysis | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets