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Terminology chevron_right Concepts chevron_right 234474009

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234474009
The component that hold information about this concept.
Dense body defect (disorder)
Dense body defect
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

Dense body defect (disorder)

SCTID: 234474009, Primitive, Active


234474009|Dense body defect (disorder)|
  • en Dense body defect
  • en Dense body defect (disorder)
  • en Storage pool deficiency

234474009 |Dense body defect (disorder)|

<<< 128099001 |Platelet storage pool defect (disorder)| :
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
          363714003 |Interprets (attribute)| = 74848003 |Hemostatic function (observable entity)| }
        { 363698007 |Finding site (attribute)| = 91689009 |Body system structure (body structure)| }
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
Active

351307011 - Dense body defect (en) View

351307011
en
Synonym (core metadata concept)
Dense body defect
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

622799013 - Dense body defect (disorder) (en) View

622799013
en
Fully specified name (core metadata concept)
Dense body defect (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

351308018 - Storage pool deficiency (en) View

351308018
en
Synonym (core metadata concept)
Storage pool deficiency
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

Relationship (4784990024) - 234474009 -> 91689009 (363698007) View

363698007 |Finding site (attribute)|
91689009 |Body system structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6999683027) - 234474009 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11290407023) - 234474009 -> 74848003 (363714003) View

363714003 |Interprets (attribute)|
74848003 |Hemostatic function (observable entity)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11290408029) - 234474009 -> 263654008 (363713009) View

363713009 |Has interpretation (attribute)|
263654008 |Abnormal (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (514131028) - 234474009 -> 16378004 (363698007) View

363698007 |Finding site (attribute)|
16378004 |Platelet (cell structure)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2712139020) - 234474009 -> 250311007 (363705008) View

363705008 |Has definitional manifestation (attribute)|
250311007 |Platelet finding (finding)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2778920021) - 234474009 -> 128153000 (363705008) View

363705008 |Has definitional manifestation (attribute)|
128153000 |Hemostatic system finding (finding)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2253637022) - 234474009 -> 57171008 (363698007) View

363698007 |Finding site (attribute)|
57171008 |Hematopoietic system structure (body structure)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (514132024) - 234474009 -> 57171008 (363698007) View

363698007 |Finding site (attribute)|
57171008 |Hematopoietic system structure (body structure)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (48164024) - 234474009 -> 128099001 (116680003) View

116680003 |Is a (attribute)|
128099001 |Platelet storage pool defect (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

128099001 View

128099001
Platelet storage pool defect (disorder)
Platelet storage pool defect
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

725034002 View

725034002
Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
Familial platelet disorder with associated myeloid malignancy
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

9311003 View

9311003
Hermansky-pudlak syndrome (disorder)
Hermansky pudlak syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

9417000 View

9417000
Platelet dense granule deficiency (disorder)
Dense body deficiency
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

36070007 View

36070007
Wiskott-aldrich syndrome (disorder)
Aldrich syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

111396008 View

111396008
Chédiak-higashi syndrome (disorder)
Chédiak anomaly
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (c6c8c325-0e79-5cb3-ba8b-73003fd07595) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D69.1
TRUE
ALWAYS D69.1
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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