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Terminology chevron_right Concepts chevron_right 702829000

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702829000
The component that hold information about this concept.
Warsaw breakage syndrome (disorder)
Warsaw breakage 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

Warsaw breakage syndrome (disorder)

SCTID: 702829000, Primitive, Active


702829000|Warsaw breakage syndrome (disorder)|
  • en Warsaw breakage syndrome
  • en Warsaw breakage syndrome (disorder)

702829000 |Warsaw breakage syndrome (disorder)|

<<< 41483000 |Multiple malformation syndrome, small stature, without skeletal dysplasia (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    363070008 |Developmental hereditary disorder (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363714003 |Interprets (attribute)| = 271603002 |Height / growth measure (observable entity)| }
Active

3006264018 - Warsaw breakage syndrome (en) View

3006264018
en
Synonym (core metadata concept)
Warsaw breakage syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

3006245012 - Warsaw breakage syndrome (disorder) (en) View

3006245012
en
Fully specified name (core metadata concept)
Warsaw breakage syndrome (disorder)
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

Relationship (13069823027) - 702829000 -> 363070008 (116680003) View

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

Relationship (13280591026) - 702829000 -> 271603002 (363714003) View

363714003 |Interprets (attribute)|
271603002 |Height / growth measure (observable entity)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (5020850021) - 702829000 -> 21390004 (116676008) View

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

Relationship (10529332023) - 702829000 -> 49755003 (116676008) View

116676008 |Associated morphology (attribute)|
49755003 |Morphologically abnormal structure (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10529333029) - 702829000 -> 308490002 (370135005) View

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

Relationship (5017900029) - 702829000 -> 41483000 (116680003) View

116680003 |Is a (attribute)|
41483000 |Multiple malformation syndrome, small stature, without skeletal dysplasia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (5017901025) - 702829000 -> 85995004 (116680003) View

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

Relationship (5017902021) - 702829000 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
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

41483000 View

41483000
Multiple malformation syndrome, small stature, without skeletal dysplasia (disorder)
Multiple malformation syndrome, small stature, without skeletal dysplasia
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

ExtendedMap object (c8bf0d18-63f0-5f3f-9874-58d28a789e24) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q87.8
TRUE
ALWAYS Q87.8
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)|
esc