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719816006: X-linked sideroblastic anemia with spinocerebellar ataxia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3318015017 X-linked sideroblastic anemia with spinocerebellar ataxia en Synonym Active Entire term case sensitive SNOMED CT core module
3318016016 X-linked sideroblastic anaemia with spinocerebellar ataxia en Synonym Active Entire term case sensitive SNOMED CT core module
3318474018 X-linked sideroblastic anemia with spinocerebellar ataxia (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked sideroblastic anemia with spinocerebellar ataxia Is a Hereditary cerebellar degeneration false Inferred relationship Existential restriction modifier
X-linked sideroblastic anemia with spinocerebellar ataxia Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
X-linked sideroblastic anemia with spinocerebellar ataxia Is a Spinocerebellar ataxia true Inferred relationship Existential restriction modifier
X-linked sideroblastic anemia with spinocerebellar ataxia Associated morphology Degeneration false Inferred relationship Existential restriction modifier 5
X-linked sideroblastic anemia with spinocerebellar ataxia Finding site Spinal cord structure false Inferred relationship Existential restriction modifier 5
X-linked sideroblastic anemia with spinocerebellar ataxia Is a Sideroblastic anemia false Inferred relationship Existential restriction modifier
X-linked sideroblastic anemia with spinocerebellar ataxia Is a Inherited disorder of porphyrin metabolism false Inferred relationship Existential restriction modifier
X-linked sideroblastic anemia with spinocerebellar ataxia Has interpretation Below reference range true Inferred relationship Existential restriction modifier 4
X-linked sideroblastic anemia with spinocerebellar ataxia Has interpretation Below reference range true Inferred relationship Existential restriction modifier 7
X-linked sideroblastic anemia with spinocerebellar ataxia Interprets Measurement of total hemoglobin concentration true Inferred relationship Existential restriction modifier 7
X-linked sideroblastic anemia with spinocerebellar ataxia Interprets Red blood cell count true Inferred relationship Existential restriction modifier 4
X-linked sideroblastic anemia with spinocerebellar ataxia Associated morphology Degeneration false Inferred relationship Existential restriction modifier 6
X-linked sideroblastic anemia with spinocerebellar ataxia Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 6
X-linked sideroblastic anemia with spinocerebellar ataxia Is a X chromosome-linked sideroblastic anemia true Inferred relationship Existential restriction modifier
X-linked sideroblastic anemia with spinocerebellar ataxia Finding site Erythrocyte true Inferred relationship Existential restriction modifier 1
X-linked sideroblastic anemia with spinocerebellar ataxia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
X-linked sideroblastic anemia with spinocerebellar ataxia Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 2
X-linked sideroblastic anemia with spinocerebellar ataxia Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 5
X-linked sideroblastic anemia with spinocerebellar ataxia Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 2
X-linked sideroblastic anemia with spinocerebellar ataxia Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 5

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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