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Terminology chevron_right Concepts chevron_right 773693005

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773693005
The component that hold information about this concept.
Spondylo-megaepiphyseal-metaphyseal dysplasia (disorder)
Spondylo-megaepiphyseal-metaphyseal dysplasia
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

Spondylo-megaepiphyseal-metaphyseal dysplasia (disorder)

SCTID: 773693005, Primitive, Active


773693005|Spondylo-megaepiphyseal-metaphyseal dysplasia (disorder)|
  • en Spondylo-megaepiphyseal-metaphyseal dysplasia
  • en Spondylo-megaepiphyseal-metaphyseal dysplasia (disorder)

773693005 |Spondylo-megaepiphyseal-metaphyseal dysplasia (disorder)|

<<< 85995004 |Autosomal recessive hereditary disorder (disorder)| +
    254062008 |Spondyloepimetaphyseal disorder (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)| }
        { 363714003 |Interprets (attribute)| = 271603002 |Height / growth measure (observable entity)| }
Active

3725806017 - Spondylo-megaepiphyseal-metaphyseal dysplasia (en) View

3725806017
en
Synonym (core metadata concept)
Spondylo-megaepiphyseal-metaphyseal dysplasia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3725808016 - Spondylo-megaepiphyseal-metaphyseal dysplasia (disorder) (en) View

3725808016
en
Fully specified name (core metadata concept)
Spondylo-megaepiphyseal-metaphyseal dysplasia (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (13070010025) - 773693005 -> 363070008 (116680003) View

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

Relationship (13280647024) - 773693005 -> 271603002 (363714003) View

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

Relationship (10618673024) - 773693005 -> 25283002 (116676008) View

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

Relationship (11225944023) - 773693005 -> 25723000 (116676008) View

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

Relationship (10618674029) - 773693005 -> 85995004 (116680003) View

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

Relationship (10618675028) - 773693005 -> 308490002 (370135005) View

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

Relationship (10618676027) - 773693005 -> 255399007 (246454002) View

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

Relationship (10618677020) - 773693005 -> 363212003 (116680003) View

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

Relationship (10618678026) - 773693005 -> 272673000 (363698007) View

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

Relationship (10618679023) - 773693005 -> 254062008 (116680003) View

116680003 |Is a (attribute)|
254062008 |Spondyloepimetaphyseal disorder (disorder)|
0
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

254062008 View

254062008
Spondyloepimetaphyseal disorder (disorder)
Spondyloepimetaphyseal disorder
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 (414391c3-43ca-5aaf-bf64-e93183ff3e8e) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q77.7
TRUE
ALWAYS Q77.7 | 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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