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Terminology chevron_right Concepts chevron_right 254158000

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Component

254158000

The component that hold information about this concept.

Fully Specified Name (FSN)

Autosomal dominant ichthyosis vulgaris (disorder)

Shortest Term

Autosomal dominant ichthyosis vulgaris

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Autosomal dominant ichthyosis vulgaris (disorder)

SCTID: 254158000, Defined, Active

254158000|Autosomal dominant ichthyosis vulgaris (disorder)|

en Autosomal dominant ichthyosis vulgaris
en Autosomal dominant ichthyosis vulgaris (disorder)
en Adi - autosomal dominant ichthyosis vulgaris

Expression

254158000 |Autosomal dominant ichthyosis vulgaris (disorder)|
 === 254157005 |Ichthyosis vulgaris (disorder)| + 
402770002 |Autosomal dominant ichthyosis (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 26996000 |Hyperkeratosis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 181469002 |Entire skin (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
363714003 |Interprets (attribute)| = 44138005 |Keratinization, function (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
378338015 - Autosomal dominant ichthyosis vulgaris (en) View
378338015	en	Synonym (core metadata concept)	Autosomal dominant ichthyosis vulgaris	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
645010017 - Autosomal dominant ichthyosis vulgaris (disorder) (en) View
645010017	en	Fully specified name (core metadata concept)	Autosomal dominant ichthyosis vulgaris (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
378339011 - ADI - Autosomal dominant ichthyosis vulgaris (en) View
378339011	en	Synonym (core metadata concept)	ADI - Autosomal dominant ichthyosis vulgaris	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (10608644027) - 254158000 -> 26996000 (116676008) View
116676008 \|Associated morphology (attribute)\|	26996000 \|Hyperkeratosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11265524023) - 254158000 -> 81845009 (116676008) View
116676008 \|Associated morphology (attribute)\|	81845009 \|Follicular hyperkeratosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11265526020) - 254158000 -> 67290009 (363698007) View
363698007 \|Finding site (attribute)\|	67290009 \|Hair follicle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12072022024) - 254158000 -> 181469002 (363698007) View
363698007 \|Finding site (attribute)\|	181469002 \|Entire skin (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1659161025) - 254158000 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3347747024) - 254158000 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11265523028) - 254158000 -> 402770002 (116680003) View
116680003 \|Is a (attribute)\|	402770002 \|Autosomal dominant ichthyosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11265525024) - 254158000 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11265527027) - 254158000 -> 44138005 (363714003) View
363714003 \|Interprets (attribute)\|	44138005 \|Keratinization, function (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4974975029) - 254158000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4974976028) - 254158000 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4997657027) - 254158000 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6126867029) - 254158000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10532387027) - 254158000 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (579800021) - 254158000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3347746026) - 254158000 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1736405023) - 254158000 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2780348021) - 254158000 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (579799022) - 254158000 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (74272029) - 254158000 -> 254157005 (116680003) View
116680003 \|Is a (attribute)\|	254157005 \|Ichthyosis vulgaris (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
402770002 View
402770002	Autosomal dominant ichthyosis (disorder)	Autosomal dominant ichthyosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
254157005 View
254157005	Ichthyosis vulgaris (disorder)	Ichthyosis vulgaris	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (e5eee4de-ffc1-5c02-b321-d451c861e022) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q80.0	TRUE	ALWAYS Q80.0	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|

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