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722006004: Isotretinoin embryopathy-like syndrome (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
3330109011 Isotretinoin embryopathy-like syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3330110018 Isotretinoin-like syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3330111019 Kawashima syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3330112014 Microtia aortic arch syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3330116012 Isotretinoin embryopathy-like syndrome 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
Isotretinoin embryopathy-like syndrome Is a Microtia true Inferred relationship Existential restriction modifier
Isotretinoin embryopathy-like syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Isotretinoin embryopathy-like syndrome Is a Congenital anomaly of aortic arch true Inferred relationship Existential restriction modifier
Isotretinoin embryopathy-like syndrome Is a Congenital anomaly of central nervous system true Inferred relationship Existential restriction modifier
Isotretinoin embryopathy-like syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Isotretinoin embryopathy-like syndrome Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier
Isotretinoin embryopathy-like syndrome Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Isotretinoin embryopathy-like syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Isotretinoin embryopathy-like syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 5
Isotretinoin embryopathy-like syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Isotretinoin embryopathy-like syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 6
Isotretinoin embryopathy-like syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 6
Isotretinoin embryopathy-like syndrome Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier 6
Isotretinoin embryopathy-like syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 7
Isotretinoin embryopathy-like syndrome Associated morphology Congenital smallness true Inferred relationship Existential restriction modifier 4
Isotretinoin embryopathy-like syndrome Finding site External ear structure true Inferred relationship Existential restriction modifier 4
Isotretinoin embryopathy-like syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 5
Isotretinoin embryopathy-like syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 7
Isotretinoin embryopathy-like syndrome Finding site Aortic arch structure false Inferred relationship Existential restriction modifier 7
Isotretinoin embryopathy-like syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Isotretinoin embryopathy-like syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Isotretinoin embryopathy-like syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Isotretinoin embryopathy-like syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Isotretinoin embryopathy-like syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Isotretinoin embryopathy-like syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Isotretinoin embryopathy-like syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Isotretinoin embryopathy-like syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4
Isotretinoin embryopathy-like syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Isotretinoin embryopathy-like syndrome Finding site Aortic arch structure true Inferred relationship Existential restriction modifier 1
Isotretinoin embryopathy-like syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Isotretinoin embryopathy-like syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 3
Isotretinoin embryopathy-like syndrome Finding site Structure of central nervous system true Inferred relationship Existential restriction modifier 2
Isotretinoin embryopathy-like syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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