Loading...
dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 716698007

Production
add
716698007
The component that hold information about this concept.
Congenital deficiency of alpha-fetoprotein (disorder)
Congenital deficiency of alpha-fetoprotein
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Congenital deficiency of alpha-fetoprotein (disorder)

SCTID: 716698007, Defined, Active


716698007|Congenital deficiency of alpha-fetoprotein (disorder)|
  • en Congenital deficiency of alpha-fetoprotein
  • en Congenital deficiency of alpha-fetoprotein (disorder)

716698007 |Congenital deficiency of alpha-fetoprotein (disorder)|

=== 66091009 |Congenital disease (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    166562001 |Alpha-fetoprotein below reference range (finding)| :
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
          363714003 |Interprets (attribute)| = 80152001 |Alpha-1-fetoprotein measurement (procedure)| }
Active

3307238016 - Congenital deficiency of alpha-fetoprotein (en) View

3307238016
en
Synonym (core metadata concept)
Congenital deficiency of alpha-fetoprotein
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3307237014 - Congenital deficiency of alpha-fetoprotein (disorder) (en) View

3307237014
en
Fully specified name (core metadata concept)
Congenital deficiency of alpha-fetoprotein (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

166562001 View

166562001
Alpha-fetoprotein below reference range (finding)
Alpha-fetoprotein low
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

85995004 View

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

ExtendedMap object (f70732ab-417a-5b1f-a552-991623acfaaf) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E88.0
TRUE
ALWAYS E88.0
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)|
esc