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68870007: Congenital dyserythropoietic anemia, type II (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
114389011 Congenital dyserythropoietic anemia, type II en Synonym Active Only initial character case insensitive SNOMED CT core module
114390019 HEMPAS en Synonym Active Entire term case sensitive SNOMED CT core module
501113010 Congenital dyserythropoietic anaemia, type II en Synonym Active Only initial character case insensitive SNOMED CT core module
808752017 Congenital dyserythropoietic anemia, type II (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
1233095010 Hereditary erythroblast multinuclearity with positive acid serum test en Synonym Active Entire term case insensitive SNOMED CT core module
1233096011 HEMPAS - Hereditary erythroblast multinuclearity with positive acid serum test 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
Congenital dyserythropoietic anemia, type II Is a Congenital dyserythropoietic anemia true Inferred relationship Existential restriction modifier
Congenital dyserythropoietic anemia, type II Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Congenital dyserythropoietic anemia, type II Occurrence Congenital true Inferred relationship Existential restriction modifier 5
Congenital dyserythropoietic anemia, type II Interprets Decreased erythrocyte production false Inferred relationship Existential restriction modifier
Congenital dyserythropoietic anemia, type II Finding site Erythrocyte true Inferred relationship Existential restriction modifier 4
Congenital dyserythropoietic anemia, type II Has definitional manifestation Decreased erythrocyte production false Inferred relationship Existential restriction modifier
Congenital dyserythropoietic anemia, type II Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Congenital dyserythropoietic anemia, type II Has definitional manifestation Erythropenia false Inferred relationship Existential restriction modifier
Congenital dyserythropoietic anemia, type II Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Congenital dyserythropoietic anemia, type II Due to Decreased erythrocyte production true Inferred relationship Existential restriction modifier 3
Congenital dyserythropoietic anemia, type II Interprets Measurement of total hemoglobin concentration true Inferred relationship Existential restriction modifier 1
Congenital dyserythropoietic anemia, type II Has interpretation Below reference range true Inferred relationship Existential restriction modifier 2
Congenital dyserythropoietic anemia, type II Has interpretation Below reference range true Inferred relationship Existential restriction modifier 1
Congenital dyserythropoietic anemia, type II 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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