dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 782752005

Production

add

Component

782752005

The component that hold information about this concept.

Fully Specified Name (FSN)

Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome (disorder)

Shortest Term

Peripheral neuropathy, myopathy, hoarseness, deafness 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

Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome (disorder)

SCTID: 782752005, Primitive, Active

782752005|Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome (disorder)|

en Peripheral neuropathy, myopathy, hoarseness, deafness syndrome
en Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome
en Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome (disorder)

Expression

782752005 |Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome (disorder)|
 <<< 232333009 |Hearing loss associated with syndrome (disorder)| + 
128283000 |Chronic nervous system disorder (disorder)| + 
128237006 |Chronic disease of musculoskeletal system (disorder)| + 
257277002 |Combined disorder of muscle and peripheral nerve (disorder)| + 
363212003 |Hereditary disorder of musculoskeletal system (disorder)| + 
60700002 |Sensorineural hearing loss (disorder)| + 
1156837002 |Autosomal dominant distal hereditary motor neuropathy (disorder)| + 
232325008 |Chronic deafness (disorder)| + 
788953003 |Hereditary hearing loss (disorder)| : 
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 117590005 |Ear structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 3058005 |Peripheral nervous system structure (body structure)| }
        { 363714003 |Interprets (attribute)| = 47078008 |Hearing, function (observable entity)| }
        { 363698007 |Finding site (attribute)| = 3057000 |Nerve structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3755615012 - Peripheral neuropathy, myopathy, hoarseness, deafness syndrome (en) View
3755615012	en	Synonym (core metadata concept)	Peripheral neuropathy, myopathy, hoarseness, deafness syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3755614011 - Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome (en) View
3755614011	en	Synonym (core metadata concept)	Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3755616013 - Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome (disorder) (en) View
3755616013	en	Fully specified name (core metadata concept)	Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11226883029) - 782752005 -> 362991006 (116680003) View
116680003 \|Is a (attribute)\|	362991006 \|Auditory system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16374478021) - 782752005 -> 788953003 (116680003) View
116680003 \|Is a (attribute)\|	788953003 \|Hereditary hearing loss (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11226875024) - 782752005 -> 128297008 (116680003) View
116680003 \|Is a (attribute)\|	128297008 \|Chronic disease of ear (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15399197025) - 782752005 -> 232325008 (116680003) View
116680003 \|Is a (attribute)\|	232325008 \|Chronic deafness (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11226873028) - 782752005 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11226876020) - 782752005 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11226885020) - 782752005 -> 302226006 (116680003) View
116680003 \|Is a (attribute)\|	302226006 \|Peripheral nerve disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11575986024) - 782752005 -> 84782009 (363698007) View
363698007 \|Finding site (attribute)\|	84782009 \|Peripheral nerve structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13824678025) - 782752005 -> 1156837002 (116680003) View
116680003 \|Is a (attribute)\|	1156837002 \|Autosomal dominant distal hereditary motor neuropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13824679022) - 782752005 -> 3058005 (363698007) View
363698007 \|Finding site (attribute)\|	3058005 \|Peripheral nervous system structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13824680020) - 782752005 -> 3057000 (363698007) View
363698007 \|Finding site (attribute)\|	3057000 \|Nerve structure (body structure)\|	6	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11226874023) - 782752005 -> 232333009 (116680003) View
116680003 \|Is a (attribute)\|	232333009 \|Hearing loss associated with syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11226878021) - 782752005 -> 128283000 (116680003) View
116680003 \|Is a (attribute)\|	128283000 \|Chronic nervous system disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11226879029) - 782752005 -> 128237006 (116680003) View
116680003 \|Is a (attribute)\|	128237006 \|Chronic disease of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11226882023) - 782752005 -> 257277002 (116680003) View
116680003 \|Is a (attribute)\|	257277002 \|Combined disorder of muscle and peripheral nerve (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11226884024) - 782752005 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11226888022) - 782752005 -> 60700002 (116680003) View
116680003 \|Is a (attribute)\|	60700002 \|Sensorineural hearing loss (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11575983027) - 782752005 -> 255314001 (263502005) View
263502005 \|Clinical course (attribute)\|	255314001 \|Progressive (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11575984022) - 782752005 -> 47078008 (363714003) View
363714003 \|Interprets (attribute)\|	47078008 \|Hearing, function (observable entity)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11575985023) - 782752005 -> 117590005 (363698007) View
363698007 \|Finding site (attribute)\|	117590005 \|Ear structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11575987026) - 782752005 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
788953003 View
788953003	Hereditary hearing loss (disorder)	Hereditary hearing loss	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
232325008 View
232325008	Chronic deafness (disorder)	Chronic deafness	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1156837002 View
1156837002	Autosomal dominant distal hereditary motor neuropathy (disorder)	Autosomal dominant distal hereditary motor neuropathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
257277002 View
257277002	Combined disorder of muscle and peripheral nerve (disorder)	Myoneural disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
60700002 View
60700002	Sensorineural hearing loss (disorder)	Mất thính giác	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
128237006 View
128237006	Chronic disease of musculoskeletal system (disorder)	Chronic musculoskeletal disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
128283000 View
128283000	Chronic nervous system disorder (disorder)	Chronic nervous system disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
232333009 View
232333009	Hearing loss associated with syndrome (disorder)	Syndromal deafness	900000000000074008 \|Necessary but not sufficient concept 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 (805e54a2-590d-55e8-ae39-40dfa799f96b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G60.0	TRUE	ALWAYS G60.0 \| 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)\|

Terminology chevron_right Concepts chevron_right 782752005

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches