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764732004: Microcephalus, cerebellar hypoplasia, cardiac conduction defect 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
3654656015 Zaki Gleeson syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3654895016 Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3654896015 Microcephaly, cerebellar hypoplasia, congenital heart conduction defect syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3654897012 Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome (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
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Is a Microcephalus false Inferred relationship Existential restriction modifier
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Is a Congenital cerebellar hypoplasia true Inferred relationship Existential restriction modifier
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Is a Intellectual disability true Inferred relationship Existential restriction modifier
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Is a Congenital conduction defect true Inferred relationship Existential restriction modifier
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 5
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Finding site Cardiac conducting system structure true Inferred relationship Existential restriction modifier 5
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 2
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 2
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Finding site Limb structure true Inferred relationship Existential restriction modifier 1
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 1
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier 3
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 3
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Associated morphology Congenital smallness true Inferred relationship Existential restriction modifier 4
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Finding site Brain structure false Inferred relationship Existential restriction modifier 4
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 5
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Is a Congenital microcephaly true Inferred relationship Existential restriction modifier
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Interprets Birth head circumference true Inferred relationship Existential restriction modifier 6
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Finding site Head structure true Inferred relationship Existential restriction modifier 4
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 6
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Interprets Intellectual ability true Inferred relationship Existential restriction modifier 7
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 7
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Interprets Adaptation behavior true Inferred relationship Existential restriction modifier 8
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 8

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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