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237985009: Pearson's syndrome (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
356688011 Pearson's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
626799011 Pearson's syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
2839083012 Pearson syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pearson's syndrome Is a Disorder of pyruvate metabolism and mitochondrial respiratory chain true Inferred relationship Existential restriction modifier
Pearson's syndrome Is a Congenital anomaly of the hematopoietic system false Inferred relationship Existential restriction modifier
Pearson's syndrome Is a Hereditary disorder of hematologic system false Inferred relationship Existential restriction modifier
Pearson's syndrome Is a Sideroblastic anemia true Inferred relationship Existential restriction modifier
Pearson's syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Pearson's syndrome Finding site Erythrocyte false Inferred relationship Existential restriction modifier
Pearson's syndrome Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Pearson's syndrome Has definitional manifestation Erythropenia false Inferred relationship Existential restriction modifier
Pearson's syndrome Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Pearson's syndrome Is a Congenital anemia false Inferred relationship Existential restriction modifier
Pearson's syndrome Is a Hereditary red blood cell disorder false Inferred relationship Existential restriction modifier
Pearson's syndrome Has interpretation Below reference range false Inferred relationship Existential restriction modifier 1
Pearson's syndrome Interprets Red blood cell count false Inferred relationship Existential restriction modifier 1
Pearson's syndrome Has interpretation Below reference range false Inferred relationship Existential restriction modifier 2
Pearson's syndrome Interprets Measurement of total hemoglobin concentration false 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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