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Terminology chevron_right Concepts chevron_right 773584001

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Component

773584001

The component that hold information about this concept.

Fully Specified Name (FSN)

Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome (disorder)

Shortest Term

Hội chứng phì đại cơ, gan to và đa ối

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

Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome (disorder)

SCTID: 773584001, Primitive, Active

773584001|Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome (disorder)|

vi Hội chứng phì đại cơ, gan to và đa ối
en Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome
en Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome (disorder)

Expression

773584001 |Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome (disorder)|
 <<< 363212003 |Hereditary disorder of musculoskeletal system (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| + 
82354003 |Multiple system malformation syndrome (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
66042003 |Congenital hyperplasia of muscle (disorder)| + 
407000 |Congenital hepatomegaly (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 442021009 |Enlargement (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 181268008 |Entire liver (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 76197007 |Hyperplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 79984008 |Skeletal muscle system structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
453471000003110 - hội chứng phì đại cơ, gan to và đa ối (vi) View
453471000003110	vi	Synonym (core metadata concept)	hội chứng phì đại cơ, gan to và đa ối	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3724292014 - Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome (en) View
3724292014	en	Synonym (core metadata concept)	Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3724293016 - Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome (disorder) (en) View
3724293016	en	Fully specified name (core metadata concept)	Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13691127026) - 773584001 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13069993022) - 773584001 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607279020) - 773584001 -> 79984008 (363698007) View
363698007 \|Finding site (attribute)\|	79984008 \|Skeletal muscle system structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607280023) - 773584001 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607281022) - 773584001 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607282026) - 773584001 -> 181268008 (363698007) View
363698007 \|Finding site (attribute)\|	181268008 \|Entire liver (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607283020) - 773584001 -> 442021009 (116676008) View
116676008 \|Associated morphology (attribute)\|	442021009 \|Enlargement (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607284025) - 773584001 -> 66042003 (116680003) View
116680003 \|Is a (attribute)\|	66042003 \|Congenital hyperplasia of muscle (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607285029) - 773584001 -> 407000 (116680003) View
116680003 \|Is a (attribute)\|	407000 \|Congenital hepatomegaly (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607286028) - 773584001 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607287021) - 773584001 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607288027) - 773584001 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607289024) - 773584001 -> 82354003 (116680003) View
116680003 \|Is a (attribute)\|	82354003 \|Multiple system malformation syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607290026) - 773584001 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11168480026) - 773584001 -> 76197007 (116676008) View
116676008 \|Associated morphology (attribute)\|	76197007 \|Hyperplasia (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
407000 View
407000	Congenital hepatomegaly (disorder)	Gan to bẩm sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
66042003 View
66042003	Congenital hyperplasia of muscle (disorder)	Doppellendigkeit	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
82354003 View
82354003	Multiple system malformation syndrome (disorder)	Multiple system malformation syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363080007 View
363080007	Digestive system hereditary disorder (disorder)	Digestive system hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363212003 View
363212003	Hereditary disorder of musculoskeletal system (disorder)	Hereditary disorder of musculoskeletal system	900000000000073002 \|Sufficiently defined by necessary conditions 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 (7a054eb9-f375-5800-81fb-8d4c5a25fd15) 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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