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Terminology chevron_right Concepts chevron_right 85557000

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Component

85557000

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary persistence of fetal hemoglobin deletion type (disorder)

Shortest Term

Hpfh deletion type

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

Hereditary persistence of fetal hemoglobin deletion type (disorder)

SCTID: 85557000, Primitive, Active

85557000|Hereditary persistence of fetal hemoglobin deletion type (disorder)|

en Hereditary persistence of fetal haemoglobin deletion type
en Hereditary persistence of fetal hemoglobin deletion type
en Hereditary persistence of fetal hemoglobin deletion type (disorder)
en Hereditary persistence of foetal haemoglobin (hpfh) deletion type
en Hereditary persistence of fetal hemoglobin (hpfh) deletion type
en Hpfh deletion type

Expression

85557000 |Hereditary persistence of fetal hemoglobin deletion type (disorder)|
 <<< 16964007 |Hereditary persistence of fetal hemoglobin thalassemia (disorder)|
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 441689006 |Measurement of total hemoglobin concentration (procedure)| }
        { 363698007 |Finding site (attribute)| = 41898006 |Erythrocyte (cell)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3013769014 - Hereditary persistence of fetal haemoglobin deletion type (en) View
3013769014	en	Synonym (core metadata concept)	Hereditary persistence of fetal haemoglobin deletion type	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
2913396019 - Hereditary persistence of fetal hemoglobin deletion type (en) View
2913396019	en	Synonym (core metadata concept)	Hereditary persistence of fetal hemoglobin deletion type	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
2913799012 - Hereditary persistence of fetal hemoglobin deletion type (disorder) (en) View
2913799012	en	Fully specified name (core metadata concept)	Hereditary persistence of fetal hemoglobin deletion type (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2612758012 - Hereditary persistence of fetal hemoglobin (HPFH) deletion type (disorder) (en) View
2612758012	en	Fully specified name (core metadata concept)	Hereditary persistence of fetal hemoglobin (HPFH) deletion type (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
2621337015 - Hereditary persistence of fetal haemoglobin (HPFH) deletion type (en) View
2621337015	en	Synonym (core metadata concept)	Hereditary persistence of fetal haemoglobin (HPFH) deletion type	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
2795252012 - Hereditary persistence of foetal haemoglobin (HPFH) deletion type (en) View
2795252012	en	Synonym (core metadata concept)	Hereditary persistence of foetal haemoglobin (HPFH) deletion type	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
2621336012 - Hereditary persistence of fetal hemoglobin (HPFH) deletion type (en) View
2621336012	en	Synonym (core metadata concept)	Hereditary persistence of fetal hemoglobin (HPFH) deletion type	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
827635016 - HPFH deletion type (disorder) (en) View
827635016	en	Fully specified name (core metadata concept)	HPFH deletion type (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	False
141806018 - HPFH deletion type (en) View
141806018	en	Synonym (core metadata concept)	HPFH deletion type	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
141807010 - HPFH deletion type, NOS (en) View
141807010	en	Synonym (core metadata concept)	HPFH deletion type, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6764254026) - 85557000 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6764255025) - 85557000 -> 441689006 (363714003) View
363714003 \|Interprets (attribute)\|	441689006 \|Measurement of total hemoglobin concentration (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6764257022) - 85557000 -> 14089001 (363714003) View
363714003 \|Interprets (attribute)\|	14089001 \|Red blood cell count (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13898402024) - 85557000 -> 441689006 (363714003) View
363714003 \|Interprets (attribute)\|	441689006 \|Measurement of total hemoglobin concentration (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (888034023) - 85557000 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7006867020) - 85557000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7006868026) - 85557000 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2270704025) - 85557000 -> 62574001 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	62574001 \|Erythropenia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6764256029) - 85557000 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3190680021) - 85557000 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2270705029) - 85557000 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (888035024) - 85557000 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (287548020) - 85557000 -> 16964007 (116680003) View
116680003 \|Is a (attribute)\|	16964007 \|Hereditary persistence of fetal hemoglobin thalassemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
16964007 View
16964007	Hereditary persistence of fetal hemoglobin thalassemia (disorder)	Hpfh	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 (006922f6-5d23-55b0-8ddf-616ff73488dd) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D56.4	TRUE	ALWAYS D56.4	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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