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Terminology chevron_right Concepts chevron_right 770679002

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Component

770679002

The component that hold information about this concept.

Fully Specified Name (FSN)

Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder)

Shortest Term

Lundberg syndrome

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

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

Summary

Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder)

SCTID: 770679002, Primitive, Active

770679002|Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder)|

en Lundberg syndrome
en Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome
en Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder)

Expression

770679002 |Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder)|
 <<< 237788002 |Premature ovarian failure (disorder)| + 
1362108000 |Genetic intellectual disability (disorder)| + 
41443008 |Multiple malformation syndrome with limb defect as major feature (disorder)| + 
42345000 |Polyneuropathy (disorder)| + 
74370006 |Micromelia (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 1303834006 |Abnormal smallness (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 243996003 |Entire limb (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 304043001 |Ovarian endocrine structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 84782009 |Peripheral nerve structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 1250004 |Decreased (qualifier value)|,
363714003 |Interprets (attribute)| = 60877009 |Hormone secretion, function (observable entity)| }
        { 363713009 |Has interpretation (attribute)| = 260379002 |Impaired (qualifier value)|,
363714003 |Interprets (attribute)| = 247573007 |Intellectual ability (observable entity)| }
        { 363713009 |Has interpretation (attribute)| = 260379002 |Impaired (qualifier value)|,
363714003 |Interprets (attribute)| = 406208005 |Adaptation behavior (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3702085019 - Lundberg syndrome (en) View
3702085019	en	Synonym (core metadata concept)	Lundberg syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3702084015 - Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (en) View
3702084015	en	Synonym (core metadata concept)	Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3702083014 - Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder) (en) View
3702083014	en	Fully specified name (core metadata concept)	Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9619399024) - 770679002 -> 110359009 (116680003) View
116680003 \|Is a (attribute)\|	110359009 \|Intellectual disability\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16317856025) - 770679002 -> 1362108000 (116680003) View
116680003 \|Is a (attribute)\|	1362108000 \|Genetic intellectual disability (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619409027) - 770679002 -> 41086002 (116676008) View
116676008 \|Associated morphology (attribute)\|	41086002 \|Congenital smallness (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15898835020) - 770679002 -> 1303834006 (116676008) View
116676008 \|Associated morphology (attribute)\|	1303834006 \|Abnormal smallness (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15094618024) - 770679002 -> 247573007 (363714003) View
363714003 \|Interprets (attribute)\|	247573007 \|Intellectual ability (observable entity)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15094619027) - 770679002 -> 260379002 (363713009) View
363713009 \|Has interpretation (attribute)\|	260379002 \|Impaired (qualifier value)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15095983025) - 770679002 -> 406208005 (363714003) View
363714003 \|Interprets (attribute)\|	406208005 \|Adaptation behavior (observable entity)\|	6	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15095984020) - 770679002 -> 260379002 (363713009) View
363713009 \|Has interpretation (attribute)\|	260379002 \|Impaired (qualifier value)\|	6	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619397021) - 770679002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619398027) - 770679002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619400028) - 770679002 -> 304043001 (363698007) View
363698007 \|Finding site (attribute)\|	304043001 \|Ovarian endocrine structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619401029) - 770679002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619402020) - 770679002 -> 74370006 (116680003) View
116680003 \|Is a (attribute)\|	74370006 \|Micromelia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619403026) - 770679002 -> 84782009 (363698007) View
363698007 \|Finding site (attribute)\|	84782009 \|Peripheral nerve structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619404021) - 770679002 -> 60877009 (363714003) View
363714003 \|Interprets (attribute)\|	60877009 \|Hormone secretion, function (observable entity)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619405022) - 770679002 -> 237788002 (116680003) View
116680003 \|Is a (attribute)\|	237788002 \|Premature ovarian failure (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619406023) - 770679002 -> 42345000 (116680003) View
116680003 \|Is a (attribute)\|	42345000 \|Polyneuropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619407025) - 770679002 -> 41443008 (116680003) View
116680003 \|Is a (attribute)\|	41443008 \|Multiple malformation syndrome with limb defect as major feature (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619408024) - 770679002 -> 1250004 (363713009) View
363713009 \|Has interpretation (attribute)\|	1250004 \|Decreased (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619410021) - 770679002 -> 243996003 (363698007) View
363698007 \|Finding site (attribute)\|	243996003 \|Entire limb (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10523468022) - 770679002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10523469025) - 770679002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10523470029) - 770679002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1362108000 View
1362108000	Genetic intellectual disability (disorder)	Genetic intellectual disability	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
74370006 View
74370006	Micromelia (disorder)	Nanomelia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
41443008 View
41443008	Multiple malformation syndrome with limb defect as major feature (disorder)	Multiple malformation syndrome with limb defect as major feature	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
42345000 View
42345000	Polyneuropathy (disorder)	Polyneuropathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
237788002 View
237788002	Premature ovarian failure (disorder)	Suy buồng trứng sớm	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 (937476a1-6a23-5ef9-83f3-e472370b31ee) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q87.8	TRUE	ALWAYS Q87.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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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