Loading...
dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 18200000

Production
add
18200000
The component that hold information about this concept.
Autosomal recessive isolated somatotropin deficiency (disorder)
Pituitary dwarfism type i
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

Autosomal recessive isolated somatotropin deficiency (disorder)

SCTID: 18200000, Primitive, Active


18200000|Autosomal recessive isolated somatotropin deficiency (disorder)|
  • en Autosomal recessive isolated somatotropin deficiency
  • en Autosomal recessive isolated somatotropin deficiency (disorder)
  • en Isolated growth hormone deficiency type i
  • en Pituitary dwarfism type i

18200000 |Autosomal recessive isolated somatotropin deficiency (disorder)|

<<< 367460001 |Pituitary dwarfism (disorder)| +
    2109003 |Isolated somatotropin deficiency (disorder)| :
        { 363698007 |Finding site (attribute)| = 52618001 |Structure of pars distalis of pituitary (body structure)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 42752001 |Due to (attribute)| = 397827003 |Growth hormone deficiency (disorder)| }
        { 363714003 |Interprets (attribute)| = 271603002 |Height / growth measure (observable entity)| }
Active

30739018 - Autosomal recessive isolated somatotropin deficiency (en) View

30739018
en
Synonym (core metadata concept)
Autosomal recessive isolated somatotropin deficiency
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

745590012 - Autosomal recessive isolated somatotropin deficiency (disorder) (en) View

745590012
en
Fully specified name (core metadata concept)
Autosomal recessive isolated somatotropin deficiency (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

30740016 - Isolated growth hormone deficiency type I (en) View

30740016
en
Synonym (core metadata concept)
Isolated growth hormone deficiency type I
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

30741017 - Pituitary dwarfism type I (en) View

30741017
en
Synonym (core metadata concept)
Pituitary dwarfism type I
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

Relationship (13280423024) - 18200000 -> 271603002 (363714003) View

363714003 |Interprets (attribute)|
271603002 |Height / growth measure (observable entity)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11577598023) - 18200000 -> 308490002 (370135005) View

370135005 |Pathological process (attribute)|
308490002 |Pathological developmental process (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (12064519029) - 18200000 -> 308490002 (370135005) View

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

Relationship (12064520024) - 18200000 -> 397827003 (42752001) View

42752001 |Due to (attribute)|
397827003 |Growth hormone deficiency (disorder)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (3037328023) - 18200000 -> 52618001 (363698007) View

363698007 |Finding site (attribute)|
52618001 |Structure of pars distalis of pituitary (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (715685022) - 18200000 -> 43451003 (116676008) View

116676008 |Associated morphology (attribute)|
43451003 |Congenital deficiency (morphologic abnormality)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2591738029) - 18200000 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (715683026) - 18200000 -> 245533002 (363698007) View

363698007 |Finding site (attribute)|
245533002 |Pars anterior of pituitary gland (body structure)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (715682020) - 18200000 -> 127944005 (363698007) View

363698007 |Finding site (attribute)|
127944005 |Entire endocrine gonad (body structure)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (715684021) - 18200000 -> 47563007 (363714003) View

363714003 |Interprets (attribute)|
47563007 |Nutritional deficiency (finding)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (175972027) - 18200000 -> 367460001 (116680003) View

116680003 |Is a (attribute)|
367460001 |Pituitary dwarfism (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (175973021) - 18200000 -> 2109003 (116680003) View

116680003 |Is a (attribute)|
2109003 |Isolated somatotropin deficiency (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

367460001 View

367460001
Pituitary dwarfism (disorder)
Pituitary nanism
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

2109003 View

2109003
Isolated somatotropin deficiency (disorder)
Isolated somatotropin deficiency
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (7b2f18b6-eff9-5083-b988-6ab46281ed96) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E23.0
TRUE
ALWAYS E23.0
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