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75443009: Hereditary elliptocytosis due to abnormal protein 4.1 (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
125306014 Hereditary elliptocytosis due to abnormal protein 4.1 en Synonym Active Entire term case insensitive SNOMED CT core module
816053017 Hereditary elliptocytosis due to abnormal protein 4.1 (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
Hereditary elliptocytosis due to abnormal protein 4.1 Is a Anemia due to intrinsic red cell abnormality true Inferred relationship Existential restriction modifier
Hereditary elliptocytosis due to abnormal protein 4.1 Is a Hereditary elliptocytosis true Inferred relationship Existential restriction modifier
Hereditary elliptocytosis due to abnormal protein 4.1 Is a Hereditary disorder of hematologic system false Inferred relationship Existential restriction modifier
Hereditary elliptocytosis due to abnormal protein 4.1 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site Erythrocyte false Inferred relationship Existential restriction modifier 3
Hereditary elliptocytosis due to abnormal protein 4.1 Has definitional manifestation Erythropenia false Inferred relationship Existential restriction modifier
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site Body system structure false Inferred relationship Existential restriction modifier
Hereditary elliptocytosis due to abnormal protein 4.1 Has interpretation Below reference range true Inferred relationship Existential restriction modifier 1
Hereditary elliptocytosis due to abnormal protein 4.1 Interprets Measurement of total hemoglobin concentration true Inferred relationship Existential restriction modifier 1
Hereditary elliptocytosis due to abnormal protein 4.1 Has interpretation Below reference range true Inferred relationship Existential restriction modifier 2
Hereditary elliptocytosis due to abnormal protein 4.1 Interprets Red blood cell count true Inferred relationship Existential restriction modifier 2
Hereditary elliptocytosis due to abnormal protein 4.1 Interprets Hemolysis true Inferred relationship Existential restriction modifier 3
Hereditary elliptocytosis due to abnormal protein 4.1 Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Hereditary elliptocytosis due to abnormal protein 4.1 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4
Hereditary elliptocytosis due to abnormal protein 4.1 Associated morphology Elliptocyte true Inferred relationship Existential restriction modifier 4
Hereditary elliptocytosis due to abnormal protein 4.1 Has interpretation Present true Inferred relationship Existential restriction modifier 3
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site Erythrocyte true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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