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Terminology chevron_right Concepts chevron_right 700211007

Production
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700211007
The component that hold information about this concept.
Ulnar mammary syndrome (disorder)
Schinzel 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

Ulnar mammary syndrome (disorder)

SCTID: 700211007, Primitive, Active


700211007|Ulnar mammary syndrome (disorder)|
  • en Ulnar mammary syndrome
  • en Ulnar-mammary syndrome
  • en Ulnar mammary syndrome (disorder)
  • en Schinzel syndrome

700211007 |Ulnar mammary syndrome (disorder)|

<<< 11164009 |Autosomal dominant hereditary disorder (disorder)| +
    37535007 |Anomaly of chromosome pair 12 (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 107673000 |Cellular and/or subcellular abnormality (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 17897000 |Chromosome pair 12 (cell structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
Active

2989585014 - Ulnar mammary syndrome (en) View

2989585014
en
Synonym (core metadata concept)
Ulnar mammary syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

2989640017 - Ulnar-mammary syndrome (en) View

2989640017
en
Synonym (core metadata concept)
Ulnar-mammary syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

2989606017 - Ulnar mammary syndrome (disorder) (en) View

2989606017
en
Fully specified name (core metadata concept)
Ulnar mammary syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

2989657018 - Schinzel syndrome (en) View

2989657018
en
Synonym (core metadata concept)
Schinzel syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

37535007 View

37535007
Anomaly of chromosome pair 12 (disorder)
Anomaly of chromosome pair 12
900000000000073002 |Sufficiently defined by necessary conditions 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

ExtendedMap object (91cf4a24-878f-5e58-944b-07ae9f7a9653) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q71.8
TRUE
ALWAYS Q71.8
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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