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Terminology chevron_right Concepts chevron_right 725036000

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Component

725036000

The component that hold information about this concept.

Fully Specified Name (FSN)

Familial isolated hypoparathyroidism (disorder)

Shortest Term

Familial isolated hypoparathyroidism

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

Familial isolated hypoparathyroidism (disorder)

SCTID: 725036000, Primitive, Active

725036000|Familial isolated hypoparathyroidism (disorder)|

en Familial isolated hypoparathyroidism
en Familial isolated hypoparathyroidism (disorder)

Expression

725036000 |Familial isolated hypoparathyroidism (disorder)|
 <<< 36976004 |Hypoparathyroidism (disorder)| + 
363104002 |Hereditary disorder of endocrine system (disorder)|
        { 363698007 |Finding site (attribute)| = 111002 |Parathyroid structure (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 1250004 |Decreased (qualifier value)|,
363714003 |Interprets (attribute)| = 60877009 |Hormone secretion, function (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3482363013 - Familial isolated hypoparathyroidism (en) View
3482363013	en	Synonym (core metadata concept)	Familial isolated hypoparathyroidism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3482362015 - Familial isolated hypoparathyroidism (disorder) (en) View
3482362015	en	Fully specified name (core metadata concept)	Familial isolated hypoparathyroidism (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (7112534021) - 725036000 -> 42497006 (116680003) View
116680003 \|Is a (attribute)\|	42497006 \|Decreased hormone secretion (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7114745021) - 725036000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7114746022) - 725036000 -> 111002 (363698007) View
363698007 \|Finding site (attribute)\|	111002 \|Parathyroid structure (body structure)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12894794023) - 725036000 -> 111002 (363698007) View
363698007 \|Finding site (attribute)\|	111002 \|Parathyroid structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12091942022) - 725036000 -> 364387009 (363714003) View
363714003 \|Interprets (attribute)\|	364387009 \|Endocrine observable (observable entity)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7112535022) - 725036000 -> 386053000 (363714003) View
363714003 \|Interprets (attribute)\|	386053000 \|Evaluation procedure (procedure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6872563027) - 725036000 -> 42497006 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	42497006 \|Decreased hormone secretion (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6872560029) - 725036000 -> 36976004 (116680003) View
116680003 \|Is a (attribute)\|	36976004 \|Hypoparathyroidism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6872561025) - 725036000 -> 363104002 (116680003) View
116680003 \|Is a (attribute)\|	363104002 \|Hereditary disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7114743025) - 725036000 -> 1250004 (363713009) View
363713009 \|Has interpretation (attribute)\|	1250004 \|Decreased (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7114744020) - 725036000 -> 60877009 (363714003) View
363714003 \|Interprets (attribute)\|	60877009 \|Hormone secretion, function (observable entity)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
36976004 View
36976004	Hypoparathyroidism (disorder)	Deficiency of pth	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363104002 View
363104002	Hereditary disorder of endocrine system (disorder)	Hereditary disorder of endocrine system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
717897007 View
717897007	Hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland (disorder)	Familial isolated hypoparathyroidism due to agenesis of parathyroid gland	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
717898002 View
717898002	Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder)	Hereditary isolated hypoparathyroidism due to impaired parathormone secretion	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
711152006 View
711152006	Autosomal dominant hypocalcemia (disorder)	Familial hypocalcemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (68158e13-a5c2-5b88-9056-7e4824fa4bd4) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E20.8	TRUE	ALWAYS E20.8 \| 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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