Loading...
dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 770947009

Production
add
770947009
The component that hold information about this concept.
Autosomal dominant severe congenital neutropenia (disorder)
Autosomal dominant severe congenital neutropenia
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

Autosomal dominant severe congenital neutropenia (disorder)

SCTID: 770947009, Primitive, Active


770947009|Autosomal dominant severe congenital neutropenia (disorder)|
  • en Autosomal dominant severe congenital neutropaenia
  • en Autosomal dominant severe congenital neutropenia
  • en Autosomal dominant severe congenital neutropenia (disorder)

770947009 |Autosomal dominant severe congenital neutropenia (disorder)|

<<< 11164009 |Autosomal dominant hereditary disorder (disorder)| +
    699346009 |Hereditary cancer-predisposing syndrome (disorder)| +
    89655007 |Congenital neutropenia (disorder)| :
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
          363714003 |Interprets (attribute)| = 30630007 |Neutrophil count (procedure)| }
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
Active

3703563012 - Autosomal dominant severe congenital neutropaenia (en) View

3703563012
en
Synonym (core metadata concept)
Autosomal dominant severe congenital neutropaenia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3703565017 - Autosomal dominant severe congenital neutropenia (en) View

3703565017
en
Synonym (core metadata concept)
Autosomal dominant severe congenital neutropenia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3703564018 - Autosomal dominant severe congenital neutropenia (disorder) (en) View

3703564018
en
Fully specified name (core metadata concept)
Autosomal dominant severe congenital neutropenia (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (9648833027) - 770947009 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11171707020) - 770947009 -> 769247005 (370135005) View

370135005 |Pathological process (attribute)|
769247005 |Abnormal immune process (qualifier value)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9648832021) - 770947009 -> 11164009 (116680003) View

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

Relationship (9648834022) - 770947009 -> 89655007 (116680003) View

116680003 |Is a (attribute)|
89655007 |Congenital neutropenia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9648835023) - 770947009 -> 281300000 (363713009) View

363713009 |Has interpretation (attribute)|
281300000 |Below reference range (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9648836024) - 770947009 -> 30630007 (363714003) View

363714003 |Interprets (attribute)|
30630007 |Neutrophil count (procedure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10721661028) - 770947009 -> 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

89655007 View

89655007
Congenital neutropenia (disorder)
Kostmann's syndrome
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (40fd4dac-1010-586a-b10c-a0ae231e5269) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D70
TRUE
ALWAYS D70 | 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)|
esc