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Terminology chevron_right Concepts chevron_right 267550008

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267550008
The component that hold information about this concept.
Congenital methemoglobinemia (disorder)
Hereditary methemoglobinemia
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

Congenital methemoglobinemia (disorder)

SCTID: 267550008, Primitive, Active


267550008|Congenital methemoglobinemia (disorder)|
  • en Hereditary methemoglobinaemia
  • en Hereditary methemoglobinemia
  • en Congenital methaemoglobinaemia
  • en Congenital methemoglobinemia
  • en Congenital methemoglobinemia (disorder)

267550008 |Congenital methemoglobinemia (disorder)|

<<< 38959009 |Methemoglobinemia (disorder)| +
    66091009 |Congenital disease (disorder)| +
    414394009 |Hereditary red blood cell disorder (disorder)| :
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 41898006 |Erythrocyte (cell)| }
Active

5460291018 - Hereditary methemoglobinaemia (en) View

5460291018
en
Synonym (core metadata concept)
Hereditary methemoglobinaemia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

5460290017 - Hereditary methemoglobinemia (en) View

5460290017
en
Synonym (core metadata concept)
Hereditary methemoglobinemia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

399256018 - Congenital methaemoglobinaemia (en) View

399256018
en
Synonym (core metadata concept)
Congenital methaemoglobinaemia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

399255019 - Congenital methemoglobinemia (en) View

399255019
en
Synonym (core metadata concept)
Congenital methemoglobinemia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

660181015 - Congenital methemoglobinemia (disorder) (en) View

660181015
en
Fully specified name (core metadata concept)
Congenital methemoglobinemia (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (16363531026) - 267550008 -> 414394009 (116680003) View

116680003 |Is a (attribute)|
414394009 |Hereditary red blood cell disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (1002521024) - 267550008 -> 41898006 (363698007) View

363698007 |Finding site (attribute)|
41898006 |Erythrocyte (cell)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (2617724024) - 267550008 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (2744787025) - 267550008 -> 250228007 (363705008) View

363705008 |Has definitional manifestation (attribute)|
250228007 |Red blood cell finding (finding)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2274608028) - 267550008 -> 57171008 (363698007) View

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

Relationship (2557675028) - 267550008 -> 40888008 (116680003) View

116680003 |Is a (attribute)|
40888008 |Congenital anomaly of the hematopoietic system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2702021023) - 267550008 -> 66091009 (116680003) View

116680003 |Is a (attribute)|
66091009 |Congenital disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (1002522028) - 267550008 -> 57171008 (363698007) View

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

Relationship (342360027) - 267550008 -> 38959009 (116680003) View

116680003 |Is a (attribute)|
38959009 |Methemoglobinemia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

414394009 View

414394009
Hereditary red blood cell disorder (disorder)
Hereditary red blood cell disorder
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

66091009 View

66091009
Congenital disease (disorder)
Congenital disease
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

38959009 View

38959009
Methemoglobinemia (disorder)
Methemoglobinemia
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

767497003 View

767497003
Autosomal recessive congenital methemoglobinemia (disorder)
Cytochrome b5 reductase deficiency
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

74912001 View

74912001
Hereditary methemoglobinemia due to globin chain mutation (disorder)
Hemoglobin m disease
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

234395000 View

234395000
Congenital methemoglobinaema with defective methemoglobin-reducing system (disorder)
Congenital methemoglobinaema with defective methemoglobin-reducing system
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (9d6a9098-1be5-597b-a94d-e0c658944284) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D74.0
TRUE
ALWAYS D74.0
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)|
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