dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 88854002

Production

add

Component

88854002

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital hypoplastic anemia (disorder)

Shortest Term

Diamond-blackfan anemia

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Congenital hypoplastic anemia (disorder)

SCTID: 88854002, Defined, Active

88854002|Congenital hypoplastic anemia (disorder)|

en Congenital pure red cell anaemia
en Congenital pure red cell anemia
en Erythrogenesis imperfecta
en Chronic constitutional pure red cell anaemia
en Chronic constitutional pure red cell anemia
en Chronic constitutional pure red cell aplasia
en Congenital erythroid hypoplasia
en Congenital hypoplastic anaemia
en Congenital hypoplastic anemia
en Congenital hypoplastic anemia (disorder)
en Congenital red cell aplasia
en Familial hypoplastic anaemia
en Familial hypoplastic anemia

Expression

88854002 |Congenital hypoplastic anemia (disorder)|
 === 40888008 |Congenital anomaly of the hematopoietic system (disorder)| + 
41614006 |Hypoplastic anemia (disorder)| + 
63565007 |Congenital anemia (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 55199003 |Hypoplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 14016003 |Bone marrow structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 441689006 |Measurement of total hemoglobin concentration (procedure)| }
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 14089001 |Red blood cell count (procedure)| }
        { 42752001 |Due to (attribute)| = 18469004 |Decreased erythrocyte production (finding)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
508245015 - Diamond-Blackfan anaemia (en) View
508245015	en	Synonym (core metadata concept)	Diamond-Blackfan anaemia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	False
147325015 - Diamond-Blackfan anemia (en) View
147325015	en	Synonym (core metadata concept)	Diamond-Blackfan anemia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	False
508243010 - Diamond-Blackfan syndrome (en) View
508243010	en	Synonym (core metadata concept)	Diamond-Blackfan syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
3664232013 - Congenital pure red cell anaemia (en) View
3664232013	en	Synonym (core metadata concept)	Congenital pure red cell anaemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3664230017 - Congenital pure red cell anemia (en) View
3664230017	en	Synonym (core metadata concept)	Congenital pure red cell anemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3664231018 - Erythrogenesis imperfecta (en) View
3664231018	en	Synonym (core metadata concept)	Erythrogenesis imperfecta	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
508246019 - Chronic constitutional pure red cell anaemia (en) View
508246019	en	Synonym (core metadata concept)	Chronic constitutional pure red cell anaemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
147326019 - Chronic constitutional pure red cell anemia (en) View
147326019	en	Synonym (core metadata concept)	Chronic constitutional pure red cell anemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
147324016 - Chronic constitutional pure red cell aplasia (en) View
147324016	en	Synonym (core metadata concept)	Chronic constitutional pure red cell aplasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
147327011 - Congenital erythroid hypoplasia (en) View
147327011	en	Synonym (core metadata concept)	Congenital erythroid hypoplasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
508244016 - Congenital hypoplastic anaemia (en) View
508244016	en	Synonym (core metadata concept)	Congenital hypoplastic anaemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
147328018 - Congenital hypoplastic anemia (en) View
147328018	en	Synonym (core metadata concept)	Congenital hypoplastic anemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2820761015 - Congenital hypoplastic anemia (disorder) (en) View
2820761015	en	Fully specified name (core metadata concept)	Congenital hypoplastic anemia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
508242017 - Congenital red cell aplasia (en) View
508242017	en	Synonym (core metadata concept)	Congenital red cell aplasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
508247011 - Familial hypoplastic anaemia (en) View
508247011	en	Synonym (core metadata concept)	Familial hypoplastic anaemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
147329014 - Familial hypoplastic anemia (en) View
147329014	en	Synonym (core metadata concept)	Familial hypoplastic anemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
831625013 - Chronic constitutional pure red cell aplasia (disorder) (en) View
831625013	en	Fully specified name (core metadata concept)	Chronic constitutional pure red cell aplasia (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (5028717027) - 88854002 -> 18469004 (42752001) View
42752001 \|Due to (attribute)\|	18469004 \|Decreased erythrocyte production (finding)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10596214025) - 88854002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (293270024) - 88854002 -> 50715003 (116680003) View
116680003 \|Is a (attribute)\|	50715003 \|Pure red cell aplasia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (897240020) - 88854002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2271005025) - 88854002 -> 62574001 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	62574001 \|Erythropenia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3348414025) - 88854002 -> 14016003 (363698007) View
363698007 \|Finding site (attribute)\|	14016003 \|Bone marrow structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6634022021) - 88854002 -> 45486003 (116676008) View
116676008 \|Associated morphology (attribute)\|	45486003 \|Aplasia (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6634023027) - 88854002 -> 52901003 (363698007) View
363698007 \|Finding site (attribute)\|	52901003 \|Structure of erythropoietic tissue (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9336878025) - 88854002 -> 40888008 (116680003) View
116680003 \|Is a (attribute)\|	40888008 \|Congenital anomaly of the hematopoietic system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9336879022) - 88854002 -> 41614006 (116680003) View
116680003 \|Is a (attribute)\|	41614006 \|Hypoplastic anemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9336884027) - 88854002 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9336886025) - 88854002 -> 14089001 (363714003) View
363714003 \|Interprets (attribute)\|	14089001 \|Red blood cell count (procedure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9340981029) - 88854002 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9340983026) - 88854002 -> 441689006 (363714003) View
363714003 \|Interprets (attribute)\|	441689006 \|Measurement of total hemoglobin concentration (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9343473020) - 88854002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9343474025) - 88854002 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (897241024) - 88854002 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3348413020) - 88854002 -> 45486003 (116676008) View
116676008 \|Associated morphology (attribute)\|	45486003 \|Aplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3572160029) - 88854002 -> 59106005 (116680003) View
116680003 \|Is a (attribute)\|	59106005 \|Anemia due to decreased red cell production (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1782107024) - 88854002 -> 18469004 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	18469004 \|Decreased erythrocyte production (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (897243022) - 88854002 -> 45486003 (116676008) View
116676008 \|Associated morphology (attribute)\|	45486003 \|Aplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1782108025) - 88854002 -> 14016003 (363698007) View
363698007 \|Finding site (attribute)\|	14016003 \|Bone marrow structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2698269024) - 88854002 -> 191268006 (116680003) View
116680003 \|Is a (attribute)\|	191268006 \|Chronic anemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2943026024) - 88854002 -> 363039000 (116680003) View
116680003 \|Is a (attribute)\|	363039000 \|Congenital connective tissue disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2943027026) - 88854002 -> 128237006 (116680003) View
116680003 \|Is a (attribute)\|	128237006 \|Chronic disease of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2950988025) - 88854002 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3053450028) - 88854002 -> 90734009 (263502005) View
263502005 \|Clinical course (attribute)\|	90734009 \|Chronic (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (897238026) - 88854002 -> 90734009 (260908002) View
260908002 \|Course (attribute)\|	90734009 \|Chronic (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2232346020) - 88854002 -> 398983000 (116680003) View
116680003 \|Is a (attribute)\|	398983000 \|Chronic disease of hematopoietic system (navigational concept)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (293267020) - 88854002 -> 128479002 (116680003) View
116680003 \|Is a (attribute)\|	128479002 \|Chronic disease of hematopoietic system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (897242028) - 88854002 -> 281833003 (363698007) View
363698007 \|Finding site (attribute)\|	281833003 \|Entire hematological system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (293266027) - 88854002 -> 363136009 (116680003) View
116680003 \|Is a (attribute)\|	363136009 \|Hereditary disorder of hematologic system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (293268026) - 88854002 -> 128289001 (116680003) View
116680003 \|Is a (attribute)\|	128289001 \|Chronic metabolic disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (293269023) - 88854002 -> 238006008 (116680003) View
116680003 \|Is a (attribute)\|	238006008 \|Disorder of purine and pyrimidine metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (897237020) - 88854002 -> 18469004 (363714003) View
363714003 \|Interprets (attribute)\|	18469004 \|Decreased erythrocyte production (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (897239023) - 88854002 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (897244027) - 88854002 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (293265028) - 88854002 -> 63565007 (116680003) View
116680003 \|Is a (attribute)\|	63565007 \|Congenital anemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
41614006 View
41614006	Hypoplastic anemia (disorder)	Hypoplastic anemia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
63565007 View
63565007	Congenital anemia (disorder)	Congenital anemia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
40888008 View
40888008	Congenital anomaly of the hematopoietic system (disorder)	Congenital anomaly of the hematopoietic system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
71988008 View
71988008	Aase syndrome (disorder)	Aase syndrome	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 (1be833e6-2b89-5bfa-b633-baf1e606f774) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D61.0	TRUE	ALWAYS D61.0	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 88854002

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches