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Terminology chevron_right Concepts chevron_right 770896003

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Melanogenesis associated transcription factor related melanoma and renal cell carcinoma predisposition syndrome (disorder)

Shortest Term

Mitf-related melanoma and renal cell carcinoma predisposition 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

Melanogenesis associated transcription factor related melanoma and renal cell carcinoma predisposition syndrome (disorder)

SCTID: 770896003, Primitive, Active

770896003|Melanogenesis associated transcription factor related melanoma and renal cell carcinoma predisposition syndrome (disorder)|

en Melanogenesis associated transcription factor related melanoma and renal cell carcinoma predisposition syndrome
en Melanogenesis associated transcription factor related melanoma and renal cell carcinoma predisposition syndrome (disorder)
en Mitf (melanogenesis associated transcription factor) related melanoma and renal cell carcinoma predisposition syndrome
en Mitf-related melanoma and renal cell carcinoma predisposition syndrome

Expression

770896003 |Melanogenesis associated transcription factor related melanoma and renal cell carcinoma predisposition syndrome (disorder)|
 <<< 699346009 |Hereditary cancer-predisposing syndrome (disorder)|

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3703314014 - Melanogenesis associated transcription factor related melanoma and renal cell carcinoma predisposition syndrome (en) View
3703314014	en	Synonym (core metadata concept)	Melanogenesis associated transcription factor related melanoma and renal cell carcinoma predisposition syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3703311018 - Melanogenesis associated transcription factor related melanoma and renal cell carcinoma predisposition syndrome (disorder) (en) View
3703311018	en	Fully specified name (core metadata concept)	Melanogenesis associated transcription factor related melanoma and renal cell carcinoma predisposition syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3703313015 - MITF (melanogenesis associated transcription factor) related melanoma and renal cell carcinoma predisposition syndrome (en) View
3703313015	en	Synonym (core metadata concept)	MITF (melanogenesis associated transcription factor) related melanoma and renal cell carcinoma predisposition syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3703312013 - MITF-related melanoma and renal cell carcinoma predisposition syndrome (en) View
3703312013	en	Synonym (core metadata concept)	MITF-related melanoma and renal cell carcinoma predisposition syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9641427023) - 770896003 -> 699346009 (116680003) View
116680003 \|Is a (attribute)\|	699346009 \|Hereditary cancer-predisposing syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
699346009 View
699346009	Hereditary cancer-predisposing syndrome (disorder)	Hereditary neoplastic syndrome	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 (62a4b73a-58ce-5096-920a-bc7cd83752d3) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	C43.9	TRUE	ALWAYS C43.9 \| POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE	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)\|
ExtendedMap object (75316e87-ffb4-53a6-96f3-80e49a6347e6) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z80.9	TRUE	ALWAYS Z80.9	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 770896003

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