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Terminology chevron_right Concepts chevron_right 725034002

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725034002
The component that hold information about this concept.
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)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)

SCTID: 725034002, Primitive, Active


725034002|Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)|
  • en Familial platelet disorder with associated myeloid malignancy
  • en Familial platelet syndrome with predisposition to acute myelogenous leukaemia
  • en Familial platelet syndrome with predisposition to acute myelogenous leukemia
  • en Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)

725034002 |Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)|

<<< 234474009 |Dense body defect (disorder)| +
    699346009 |Hereditary cancer-predisposing syndrome (disorder)| +
    11164009 |Autosomal dominant hereditary disorder (disorder)| :
        { 363698007 |Finding site (attribute)| = 414387006 |Structure of hematological system (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
          363714003 |Interprets (attribute)| = 74848003 |Hemostatic function (observable entity)| }
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
Active

3437138013 - Familial platelet disorder with associated myeloid malignancy (en) View

3437138013
en
Synonym (core metadata concept)
Familial platelet disorder with associated myeloid malignancy
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

3437137015 - Familial platelet syndrome with predisposition to acute myelogenous leukaemia (en) View

3437137015
en
Synonym (core metadata concept)
Familial platelet syndrome with predisposition to acute myelogenous leukaemia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3437136012 - Familial platelet syndrome with predisposition to acute myelogenous leukemia (en) View

3437136012
en
Synonym (core metadata concept)
Familial platelet syndrome with predisposition to acute myelogenous leukemia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3437135011 - Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder) (en) View

3437135011
en
Fully specified name (core metadata concept)
Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (6872551021) - 725034002 -> 414387006 (363698007) View

363698007 |Finding site (attribute)|
414387006 |Structure of hematological system (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (11571754026) - 725034002 -> 263654008 (363713009) View

363713009 |Has interpretation (attribute)|
263654008 |Abnormal (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (12436943028) - 725034002 -> 414387006 (363698007) View

363698007 |Finding site (attribute)|
414387006 |Structure of hematological system (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12436944023) - 725034002 -> 263654008 (363713009) View

363713009 |Has interpretation (attribute)|
263654008 |Abnormal (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6999766025) - 725034002 -> 255399007 (246454002) View

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

Relationship (11571755025) - 725034002 -> 74848003 (363714003) View

363714003 |Interprets (attribute)|
74848003 |Hemostatic function (observable entity)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6872548025) - 725034002 -> 11164009 (116680003) View

116680003 |Is a (attribute)|
11164009 |Autosomal dominant hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6872549022) - 725034002 -> 234474009 (116680003) View

116680003 |Is a (attribute)|
234474009 |Dense body defect (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6872550022) - 725034002 -> 699346009 (116680003) View

116680003 |Is a (attribute)|
699346009 |Hereditary cancer-predisposing syndrome (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

699346009 View

699346009
Hereditary cancer-predisposing syndrome (disorder)
Hereditary neoplastic syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

11164009 View

11164009
Autosomal dominant hereditary disorder (disorder)
Ad - autosomal dominant
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

234474009 View

234474009
Dense body defect (disorder)
Dense body defect
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (070da274-2030-5250-85dc-c2fd8c50cb53) View

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

ExtendedMap object (d3398fcf-2514-5918-b630-056647aefc01) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D69.4
TRUE
ALWAYS D69.4 | 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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