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234371002: Congenital pure red cell aplasia (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    351128013 Congenital pure red cell aplasia en Synonym Active Entire term case insensitive SNOMED CT core module
    622680012 Congenital pure red cell aplasia (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
    Congenital pure red cell aplasia Is a Pure red cell aplasia false Inferred relationship Existential restriction modifier
    Congenital pure red cell aplasia Associated morphology Aplasia false Inferred relationship Existential restriction modifier 1
    Congenital pure red cell aplasia Finding site Entire hematological system false Inferred relationship Existential restriction modifier 1
    Congenital pure red cell aplasia Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
    Congenital pure red cell aplasia Interprets Decreased erythrocyte production false Inferred relationship Existential restriction modifier
    Congenital pure red cell aplasia Finding site Erythrocyte false Inferred relationship Existential restriction modifier
    Congenital pure red cell aplasia Finding site Bone marrow structure false Inferred relationship Existential restriction modifier 1
    Congenital pure red cell aplasia Has definitional manifestation Decreased erythrocyte production false Inferred relationship Existential restriction modifier
    Congenital pure red cell aplasia Has definitional manifestation Erythropenia false Inferred relationship Existential restriction modifier
    Congenital pure red cell aplasia Is a Congenital anomaly of the hematopoietic system false Inferred relationship Existential restriction modifier
    Congenital pure red cell aplasia Occurrence Congenital false Inferred relationship Existential restriction modifier
    Congenital pure red cell aplasia Is a Congenital anemia false Inferred relationship Existential restriction modifier
    Congenital pure red cell aplasia Is a Congenital connective tissue disorder false Inferred relationship Existential restriction modifier
    Congenital pure red cell aplasia Finding site Bone structure false Inferred relationship Existential restriction modifier
    Congenital pure red cell aplasia Associated morphology Aplasia false Inferred relationship Existential restriction modifier 1
    Congenital pure red cell aplasia Finding site Bone marrow structure false Inferred relationship Existential restriction modifier 1
    Congenital pure red cell aplasia Due to Decreased erythrocyte production false Inferred relationship Existential restriction modifier
    Congenital pure red cell aplasia Is a Anemia false Inferred relationship Existential restriction modifier
    Congenital pure red cell aplasia Associated morphology Aplasia false Inferred relationship Existential restriction modifier 2
    Congenital pure red cell aplasia Finding site Structure of erythropoietic tissue false Inferred relationship Existential restriction modifier 2
    Congenital pure red cell aplasia Is a Red blood cell disorder false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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