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Terminology chevron_right Concepts chevron_right 718559000

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718559000
The component that hold information about this concept.
Acromesomelic dysplasia maroteaux type (disorder)
Acromesomelic dysplasia maroteaux type
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

Acromesomelic dysplasia maroteaux type (disorder)

SCTID: 718559000, Primitive, Active


718559000|Acromesomelic dysplasia maroteaux type (disorder)|
  • en Acromesomelic dysplasia maroteaux type
  • en Acromesomelic dysplasia maroteaux type (disorder)

718559000 |Acromesomelic dysplasia maroteaux type (disorder)|

<<< 85995004 |Autosomal recessive hereditary disorder (disorder)| +
    279082008 |Acromesomelic dysplasia group (disorder)| +
    363212003 |Hereditary disorder of musculoskeletal system (disorder)| +
    363070008 |Developmental hereditary disorder (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 25723000 |Dysplasia (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 272673000 |Bone structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
Active

3312763019 - Acromesomelic dysplasia Maroteaux type (en) View

3312763019
en
Synonym (core metadata concept)
Acromesomelic dysplasia Maroteaux type
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3312762012 - Acromesomelic dysplasia Maroteaux type (disorder) (en) View

3312762012
en
Fully specified name (core metadata concept)
Acromesomelic dysplasia Maroteaux type (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

Relationship (13069072022) - 718559000 -> 363070008 (116680003) View

116680003 |Is a (attribute)|
363070008 |Developmental hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6611182029) - 718559000 -> 25283002 (116676008) View

116676008 |Associated morphology (attribute)|
25283002 |Congenital dysplasia (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (11224963028) - 718559000 -> 25723000 (116676008) View

116676008 |Associated morphology (attribute)|
25723000 |Dysplasia (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6611180021) - 718559000 -> 363045008 (116680003) View

116680003 |Is a (attribute)|
363045008 |Connective tissue hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (10521580022) - 718559000 -> 308490002 (370135005) View

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

Relationship (6611178026) - 718559000 -> 85995004 (116680003) View

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

Relationship (6611179023) - 718559000 -> 279082008 (116680003) View

116680003 |Is a (attribute)|
279082008 |Acromesomelic dysplasia group (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6611181020) - 718559000 -> 363212003 (116680003) View

116680003 |Is a (attribute)|
363212003 |Hereditary disorder of musculoskeletal system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6611183023) - 718559000 -> 255399007 (246454002) View

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

Relationship (6611184028) - 718559000 -> 272673000 (363698007) View

363698007 |Finding site (attribute)|
272673000 |Bone structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

363070008 View

363070008
Developmental hereditary disorder (disorder)
Developmental hereditary disorder
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

279082008 View

279082008
Acromesomelic dysplasia group (disorder)
Acromesomelic dwarfism
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

363212003 View

363212003
Hereditary disorder of musculoskeletal system (disorder)
Hereditary disorder of musculoskeletal system
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (f19db65c-11b5-54aa-8ae9-8e7da148c844) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q77.8
TRUE
ALWAYS Q77.8 | 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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