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Terminology chevron_right Concepts chevron_right 702364003

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702364003
The component that hold information about this concept.
Chylomicron retention disease (disorder)
Anderson syndrome
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

Chylomicron retention disease (disorder)

SCTID: 702364003, Primitive, Active


702364003|Chylomicron retention disease (disorder)|
  • en Anderson syndrome
  • en Chylomicron retention disease
  • en Chylomicron retention disease (disorder)
  • en Lipid transport defect of intestine

702364003 |Chylomicron retention disease (disorder)|

<<< 85995004 |Autosomal recessive hereditary disorder (disorder)| +
    197494007 |Intestinal malabsorption of fat (disorder)| +
    363080007 |Digestive system hereditary disorder (disorder)| +
    42357009 |Disorder of digestive system specific to fetus or newborn (disorder)| +
    60193003 |Familial hypobetalipoproteinemia (disorder)| :
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 30315005 |Small intestinal structure (body structure)| }
Active

2995599016 - Anderson syndrome (en) View

2995599016
en
Synonym (core metadata concept)
Anderson syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

2995184011 - Chylomicron retention disease (en) View

2995184011
en
Synonym (core metadata concept)
Chylomicron retention disease
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

2995490019 - Chylomicron retention disease (disorder) (en) View

2995490019
en
Fully specified name (core metadata concept)
Chylomicron retention disease (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

2995232014 - Lipid transport defect of intestine (en) View

2995232014
en
Synonym (core metadata concept)
Lipid transport defect of intestine
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

Relationship (16344129029) - 702364003 -> 197494007 (116680003) View

116680003 |Is a (attribute)|
197494007 |Intestinal malabsorption of fat (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (16344130023) - 702364003 -> 363080007 (116680003) View

116680003 |Is a (attribute)|
363080007 |Digestive system hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (16344131022) - 702364003 -> 42357009 (116680003) View

116680003 |Is a (attribute)|
42357009 |Disorder of digestive system specific to fetus or newborn (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (16344132026) - 702364003 -> 60193003 (116680003) View

116680003 |Is a (attribute)|
60193003 |Familial hypobetalipoproteinemia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (16344133020) - 702364003 -> 255399007 (246454002) View

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

Relationship (16344134025) - 702364003 -> 30315005 (363698007) View

363698007 |Finding site (attribute)|
30315005 |Small intestinal structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (4968170025) - 702364003 -> 85995004 (116680003) View

116680003 |Is a (attribute)|
85995004 |Autosomal recessive hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

42357009 View

42357009
Disorder of digestive system specific to fetus or newborn (disorder)
Perinatal digestive system disorders
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

60193003 View

60193003
Familial hypobetalipoproteinemia (disorder)
Familial hypobetalipoproteinemia
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

85995004 View

85995004
Autosomal recessive hereditary disorder (disorder)
Hereditary disorder trait, nos
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

197494007 View

197494007
Intestinal malabsorption of fat (disorder)
Intestinal malabsorption of fat
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

363080007 View

363080007
Digestive system hereditary disorder (disorder)
Digestive system hereditary disorder
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (e067a307-ad23-5d5b-a59f-8aa69c525a62) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E78.6
TRUE
ALWAYS E78.6 | 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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