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733049004: Encephalopathy, intracerebral calcification, retinal degeneration syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3498634010 Encephalopathy, intracerebral calcification, retinal degeneration syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3498635011 Encephalopathy, intracerebral calcification, retinal degeneration syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3498636012 Bonnemann Meinecke Reich syndrome 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
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Is a Cerebral calcification true Inferred relationship Existential restriction modifier
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Is a Mental retardation false Inferred relationship Existential restriction modifier
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Is a Degeneration of retina true Inferred relationship Existential restriction modifier
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Associated morphology Degeneration false Inferred relationship Existential restriction modifier 5
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Finding site Retinal structure false Inferred relationship Existential restriction modifier 5
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Associated morphology Pathologic calcification, calcified structure false Inferred relationship Existential restriction modifier 4
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Finding site Structure of cerebrum false Inferred relationship Existential restriction modifier 4
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Is a Intellectual disability true Inferred relationship Existential restriction modifier
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Is a Anomalies of cerebrum false Inferred relationship Existential restriction modifier
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Is a Congenital anomaly of retina true Inferred relationship Existential restriction modifier
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Associated morphology Degeneration false Inferred relationship Existential restriction modifier 2
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Finding site Structure of cerebrum true Inferred relationship Existential restriction modifier 1
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Associated morphology Pathologic calcification, calcified structure true Inferred relationship Existential restriction modifier 1
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Finding site Retinal structure true Inferred relationship Existential restriction modifier 2
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Is a Congenital anomaly of cerebrum true Inferred relationship Existential restriction modifier
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Is a Congenital degeneration of nervous system true Inferred relationship Existential restriction modifier
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 2
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Interprets Intellectual ability true Inferred relationship Existential restriction modifier 3
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 3
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Interprets Adaptation behavior true Inferred relationship Existential restriction modifier 4
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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