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Terminology chevron_right Concepts chevron_right 763401009

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763401009
The component that hold information about this concept.
Ichthyosis prematurity syndrome (disorder)
Congenital ichthyosis type 4
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

Ichthyosis prematurity syndrome (disorder)

SCTID: 763401009, Primitive, Active


763401009|Ichthyosis prematurity syndrome (disorder)|
  • en Congenital ichthyosis type 4
  • en Ichthyosis prematurity syndrome
  • en Ichthyosis prematurity syndrome (disorder)

763401009 |Ichthyosis prematurity syndrome (disorder)|

<<< 402772005 |Autosomal recessive ichthyosis (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 26996000 |Hyperkeratosis (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 181469002 |Entire skin (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
          363714003 |Interprets (attribute)| = 44138005 |Keratinization, function (observable entity)| }
Active

3642106015 - Congenital ichthyosis type 4 (en) View

3642106015
en
Synonym (core metadata concept)
Congenital ichthyosis type 4
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

3642107012 - Ichthyosis prematurity syndrome (en) View

3642107012
en
Synonym (core metadata concept)
Ichthyosis prematurity syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3642108019 - Ichthyosis prematurity syndrome (disorder) (en) View

3642108019
en
Fully specified name (core metadata concept)
Ichthyosis prematurity syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (9102461028) - 763401009 -> 39937001 (363698007) View

363698007 |Finding site (attribute)|
39937001 |Skin structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (12392138023) - 763401009 -> 181469002 (363698007) View

363698007 |Finding site (attribute)|
181469002 |Entire skin (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9102457023) - 763401009 -> 13059002 (116680003) View

116680003 |Is a (attribute)|
13059002 |Congenital ichthyosis of skin (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (9102458029) - 763401009 -> 85995004 (116680003) View

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

Relationship (11265579026) - 763401009 -> 402772005 (116680003) View

116680003 |Is a (attribute)|
402772005 |Autosomal recessive ichthyosis (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11265580028) - 763401009 -> 263654008 (363713009) View

363713009 |Has interpretation (attribute)|
263654008 |Abnormal (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11265581029) - 763401009 -> 44138005 (363714003) View

363714003 |Interprets (attribute)|
44138005 |Keratinization, function (observable entity)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9102459021) - 763401009 -> 21390004 (116676008) View

116676008 |Associated morphology (attribute)|
21390004 |Developmental anomaly (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (10514846028) - 763401009 -> 308490002 (370135005) View

370135005 |Pathological process (attribute)|
308490002 |Pathological developmental process (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10608585027) - 763401009 -> 26996000 (116676008) View

116676008 |Associated morphology (attribute)|
26996000 |Hyperkeratosis (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9102460027) - 763401009 -> 255399007 (246454002) View

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

402772005 View

402772005
Autosomal recessive ichthyosis (disorder)
Autosomal recessive ichthyosis
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (7c544b32-2be5-5857-b145-8b6fd97ebfbd) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q82.8
TRUE
ALWAYS Q82.8 | 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)|

ExtendedMap object (e3405ab3-aa33-514c-ac87-bd601bd2e600) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q80.8
TRUE
ALWAYS Q80.8 | 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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