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771439009: 14q22q23 microdeletion syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3706197018 Monosomy 14q22q23 en Synonym Active Entire term case insensitive SNOMED CT core module
3706198011 14q22q23 microdeletion syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3706199015 14q22-q23 microdeletion syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3706200017 Monosomy 14q22-q23 en Synonym Active Entire term case insensitive SNOMED CT core module
3706201018 14q22q23 microdeletion 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
14q22q23 microdeletion syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier
14q22q23 microdeletion syndrome Finding site Structure of visual system true Inferred relationship Existential restriction modifier 3
14q22q23 microdeletion syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
14q22q23 microdeletion syndrome Is a Deletion of part of chromosome 14 false Inferred relationship Existential restriction modifier
14q22q23 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
14q22q23 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
14q22q23 microdeletion syndrome Finding site Chromosome pair 14 false Inferred relationship Existential restriction modifier 4
14q22q23 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
14q22q23 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 4
14q22q23 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
14q22q23 microdeletion syndrome Finding site Limb structure true Inferred relationship Existential restriction modifier 1
14q22q23 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
14q22q23 microdeletion syndrome Finding site Long arm of chromosome false Inferred relationship Existential restriction modifier 2
14q22q23 microdeletion syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
14q22q23 microdeletion syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 5
14q22q23 microdeletion syndrome Is a Disorder of extremity false Inferred relationship Existential restriction modifier
14q22q23 microdeletion syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 5
14q22q23 microdeletion syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 5
14q22q23 microdeletion syndrome Is a Visual system disorder false Inferred relationship Existential restriction modifier
14q22q23 microdeletion syndrome Is a Congenital anomaly of visual system true Inferred relationship Existential restriction modifier
14q22q23 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
14q22q23 microdeletion syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
14q22q23 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
14q22q23 microdeletion syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
14q22q23 microdeletion syndrome Is a Congenital anomaly of limb true Inferred relationship Existential restriction modifier
14q22q23 microdeletion syndrome Is a Partial deletion of long arm of chromosome 14 true Inferred relationship Existential restriction modifier
14q22q23 microdeletion syndrome Finding site Chromosome pair 14 true Inferred relationship Existential restriction modifier 2
14q22q23 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
14q22q23 microdeletion syndrome Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 4
14q22q23 microdeletion syndrome Pathological process Pathological developmental process 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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