FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

178935009: Congenital elliptocytosis (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    276861015 Congenital elliptocytosis en Synonym Active Entire term case insensitive SNOMED CT core module
    276862010 Congenital ovalocytosis en Synonym Active Entire term case insensitive SNOMED CT core module
    561898014 Congenital elliptocytosis (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 elliptocytosis Is a Hereditary disorder of hematologic system false Inferred relationship Existential restriction modifier
    Congenital elliptocytosis Is a Erythrocyte membrane abnormality false Inferred relationship Existential restriction modifier
    Congenital elliptocytosis Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
    Congenital elliptocytosis Finding site Erythrocyte false Inferred relationship Existential restriction modifier
    Congenital elliptocytosis Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
    Congenital elliptocytosis Is a Congenital anomaly of the hematopoietic system false Inferred relationship Existential restriction modifier
    Congenital elliptocytosis Occurrence Congenital false Inferred relationship Existential restriction modifier
    Congenital elliptocytosis Is a Hereditary disease false Inferred relationship Existential restriction modifier
    Congenital elliptocytosis Is a Congenital disease false Inferred relationship Existential restriction modifier
    Congenital elliptocytosis Has definitional manifestation Red blood cell finding false Inferred relationship Existential restriction modifier
    Congenital elliptocytosis Is a Congenital malformation false Inferred relationship Existential restriction modifier
    Congenital elliptocytosis Is a Hereditary red blood cell disorder false Inferred relationship Existential restriction modifier
    Congenital elliptocytosis Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Congenital elliptocytosis Associated morphology Congenital abnormal shape false Inferred relationship Existential restriction modifier 1
    Congenital elliptocytosis Finding site Erythrocyte false Inferred relationship Existential restriction modifier 1
    Congenital elliptocytosis Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Congenital elliptocytosis Associated morphology Abnormal shape false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

    Back to Start