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722006004: Isotretinoin embryopathy-like syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3330109011 Isotretinoin embryopathy-like syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330110018 Isotretinoin-like syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330111019 Kawashima syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3330112014 Microtia aortic arch syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330116012 Isotretinoin embryopathy-like syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5402768018 Isotretinoin-like syndrome is a phenocopy of the isotretinoin embryopathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Isotretinoin embryopathy-like syndrome (disorder) Is a Microtia true Inferred relationship Some
Isotretinoin embryopathy-like syndrome (disorder) Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Isotretinoin embryopathy-like syndrome (disorder) Is a Congenital anomaly of aortic arch true Inferred relationship Some
Isotretinoin embryopathy-like syndrome (disorder) Is a Congenital anomaly of central nervous system true Inferred relationship Some
Isotretinoin embryopathy-like syndrome (disorder) Is a Auditory system hereditary disorder true Inferred relationship Some
Isotretinoin embryopathy-like syndrome (disorder) Is a Cardiovascular system hereditary disorder true Inferred relationship Some
Isotretinoin embryopathy-like syndrome (disorder) Is a Hereditary disorder of nervous system true Inferred relationship Some
Isotretinoin embryopathy-like syndrome (disorder) Occurrence Congenital true Inferred relationship Some 4
Isotretinoin embryopathy-like syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 5
Isotretinoin embryopathy-like syndrome (disorder) Occurrence Congenital false Inferred relationship Some 5
Isotretinoin embryopathy-like syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 6
Isotretinoin embryopathy-like syndrome (disorder) Occurrence Congenital false Inferred relationship Some 6
Isotretinoin embryopathy-like syndrome (disorder) Finding site Structure of central nervous system (body structure) false Inferred relationship Some 6
Isotretinoin embryopathy-like syndrome (disorder) Occurrence Congenital false Inferred relationship Some 7
Isotretinoin embryopathy-like syndrome (disorder) Associated morphology Congenital smallness false Inferred relationship Some 4
Isotretinoin embryopathy-like syndrome (disorder) Finding site External ear structure true Inferred relationship Some 4
Isotretinoin embryopathy-like syndrome (disorder) Finding site Face structure false Inferred relationship Some 5
Isotretinoin embryopathy-like syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 7
Isotretinoin embryopathy-like syndrome (disorder) Finding site Aortic arch structure false Inferred relationship Some 7
Isotretinoin embryopathy-like syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Isotretinoin embryopathy-like syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Isotretinoin embryopathy-like syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Isotretinoin embryopathy-like syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Isotretinoin embryopathy-like syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Isotretinoin embryopathy-like syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Isotretinoin embryopathy-like syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Isotretinoin embryopathy-like syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Isotretinoin embryopathy-like syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
Isotretinoin embryopathy-like syndrome (disorder) Finding site Aortic arch structure true Inferred relationship Some 1
Isotretinoin embryopathy-like syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Isotretinoin embryopathy-like syndrome (disorder) Finding site Face structure true Inferred relationship Some 3
Isotretinoin embryopathy-like syndrome (disorder) Finding site Structure of central nervous system (body structure) true Inferred relationship Some 2
Isotretinoin embryopathy-like syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Isotretinoin embryopathy-like syndrome (disorder) Associated morphology Abnormal smallness (morphologic abnormality) true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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