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29177004: Anemia due to pentose phosphate pathway defect (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
48823016 Anemia due to pentose phosphate pathway defect en Synonym Active Entire term case insensitive SNOMED CT core module
484230011 Anaemia due to pentose phosphate pathway defect en Synonym Active Entire term case insensitive SNOMED CT core module
760041013 Anemia due to pentose phosphate pathway defect (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anemia due to pentose phosphate pathway defect Is a Anemia due to enzyme deficiency true Inferred relationship Existential restriction modifier
Anemia due to pentose phosphate pathway defect Finding site Erythrocyte false Inferred relationship Existential restriction modifier 4
Anemia due to pentose phosphate pathway defect Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Anemia due to pentose phosphate pathway defect Associated etiologic finding Enzymopathy false Inferred relationship Existential restriction modifier
Anemia due to pentose phosphate pathway defect Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Anemia due to pentose phosphate pathway defect Has definitional manifestation Erythropenia false Inferred relationship Existential restriction modifier
Anemia due to pentose phosphate pathway defect Due to Enzymopathy true Inferred relationship Existential restriction modifier 5
Anemia due to pentose phosphate pathway defect Has definitional manifestation Hemolysis false Inferred relationship Existential restriction modifier
Anemia due to pentose phosphate pathway defect Has interpretation Below reference range false Inferred relationship Existential restriction modifier 1
Anemia due to pentose phosphate pathway defect Has interpretation Below reference range true Inferred relationship Existential restriction modifier 2
Anemia due to pentose phosphate pathway defect Interprets Red blood cell count false Inferred relationship Existential restriction modifier 1
Anemia due to pentose phosphate pathway defect Interprets Measurement of total hemoglobin concentration false Inferred relationship Existential restriction modifier 2
Anemia due to pentose phosphate pathway defect Interprets Erythrocyte destruction, function false Inferred relationship Existential restriction modifier
Anemia due to pentose phosphate pathway defect Has interpretation Present false Inferred relationship Existential restriction modifier 3
Anemia due to pentose phosphate pathway defect Interprets Hemolysis false Inferred relationship Existential restriction modifier 3
Anemia due to pentose phosphate pathway defect Interprets Hemolysis true Inferred relationship Existential restriction modifier 1
Anemia due to pentose phosphate pathway defect Has interpretation Present true Inferred relationship Existential restriction modifier 1
Anemia due to pentose phosphate pathway defect Interprets Red blood cell count true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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