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768556005: Ataxia pancytopenia syndrome (disorder)

Status: current, 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
3686039019 Ataxia pancytopenia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3686040017 Ataxia pancytopenia syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3686041018 Myelocerebellar disorder en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ataxia pancytopenia syndrome Is a Hereditary ataxia true Inferred relationship Existential restriction modifier
Ataxia pancytopenia syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Ataxia pancytopenia syndrome Is a Hereditary white blood cell disorder true Inferred relationship Existential restriction modifier
Ataxia pancytopenia syndrome Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 5
Ataxia pancytopenia syndrome Is a Pancytopenia true Inferred relationship Existential restriction modifier
Ataxia pancytopenia syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 1
Ataxia pancytopenia syndrome Interprets Red blood cell count true Inferred relationship Existential restriction modifier 4
Ataxia pancytopenia syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 2
Ataxia pancytopenia syndrome Is a Inherited platelet disorder true Inferred relationship Existential restriction modifier
Ataxia pancytopenia syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 4
Ataxia pancytopenia syndrome Is a Cerebellar ataxia true Inferred relationship Existential restriction modifier
Ataxia pancytopenia syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 3
Ataxia pancytopenia syndrome Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Ataxia pancytopenia syndrome Interprets White blood cell count true Inferred relationship Existential restriction modifier 1
Ataxia pancytopenia syndrome Interprets Platelet count true Inferred relationship Existential restriction modifier 3
Ataxia pancytopenia syndrome Interprets Measurement of total hemoglobin concentration true Inferred relationship Existential restriction modifier 2
Ataxia pancytopenia syndrome Pathological process Abnormal immune process true Inferred relationship Existential restriction modifier 7
Ataxia pancytopenia syndrome Is a Functional finding false Inferred relationship Existential restriction modifier
Ataxia pancytopenia syndrome Interprets Hemostatic function false Inferred relationship Existential restriction modifier 6
Ataxia pancytopenia syndrome Has interpretation Abnormal false Inferred relationship Existential restriction modifier 6
Ataxia pancytopenia syndrome Interprets Hemostatic function true Inferred relationship Existential restriction modifier 6
Ataxia pancytopenia syndrome Has interpretation Abnormal true Inferred relationship Existential restriction modifier 6
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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