Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
87546013 |
Steroid 21-monooxygenase deficiency, simple virilizing type |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
87548014 |
Simple virilizing adrenal hyperplasia |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
87549018 |
Adrenogenital disorder due to 21-hydroxylase deficiency |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
87550018 |
Congenital adrenal hyperplasia, type 1 |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
496368011 |
Steroid 21-monooxygenase deficiency, simple virilising type |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
496369015 |
Simple-virilising congenital adrenal hyperplasia |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
496370019 |
Simple virilising adrenal hyperplasia |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
496372010 |
Simple-virilizing congenital adrenal hyperplasia |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
790632010 |
Steroid 21-monooxygenase deficiency, simple virilizing type (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
1783827016 |
Steroid 21-hydroxylase deficiency, simple virilising type |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
1784215016 |
Steroid 21-hydroxylase deficiency, simple virilizing type |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
87546013 |
Steroid 21-monooxygenase deficiency, simple virilizing type |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
87546013 |
Steroid 21-monooxygenase deficiency, simple virilizing type |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
87548014 |
Simple virilizing adrenal hyperplasia |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
87548014 |
Simple virilizing adrenal hyperplasia |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
87549018 |
Adrenogenital disorder due to 21-hydroxylase deficiency |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
87549018 |
Adrenogenital disorder due to 21-hydroxylase deficiency |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
87550018 |
Congenital adrenal hyperplasia, type 1 |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
87550018 |
Congenital adrenal hyperplasia, type 1 |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
198397017 |
Steroid 21-hydroxylase deficiency, simiple virilizing type |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
496368011 |
Steroid 21-monooxygenase deficiency, simple virilising type |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
496368011 |
Steroid 21-monooxygenase deficiency, simple virilising type |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
496369015 |
Simple-virilising congenital adrenal hyperplasia |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
496369015 |
Simple-virilising congenital adrenal hyperplasia |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
496370019 |
Simple virilising adrenal hyperplasia |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
496370019 |
Simple virilising adrenal hyperplasia |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
496371015 |
Steroid 21-hydroxylase deficiency, simiple virilising type |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
496372010 |
Simple-virilizing congenital adrenal hyperplasia |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
496372010 |
Simple-virilizing congenital adrenal hyperplasia |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
790632010 |
Steroid 21-monooxygenase deficiency, simple virilizing type (disorder) |
en |
Fully specified name |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
790632010 |
Steroid 21-monooxygenase deficiency, simple virilizing type (disorder) |
en |
Fully specified name |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
1783827016 |
Steroid 21-hydroxylase deficiency, simple virilising type |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
1783827016 |
Steroid 21-hydroxylase deficiency, simple virilising type |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
1784215016 |
Steroid 21-hydroxylase deficiency, simple virilizing type |
en |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
SNOMED CT core |
1784215016 |
Steroid 21-hydroxylase deficiency, simple virilizing type |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
4561651000241114 |
déficit en stéroïde 21-mono-oxygénase de type virilisant |
fr |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
4561651000241114 |
déficit en stéroïde 21-mono-oxygénase de type virilisant |
fr |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships |
Type |
Target |
Active |
Characteristic |
Refinability |
Group |
Values |
Steroid 21-monooxygenase deficiency, simple virilizing type |
Is a |
Congenital anomaly of adrenal gland |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Is a |
Inborn error of metabolism |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Is a |
Adrenal virilism |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Is a |
Enzymopathy |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Is a |
Hereditary disorder of endocrine system (disorder) |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Is a |
Congenital adrenal hyperplasia |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Is a |
Reproductive system hereditary disorder (disorder) |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Is a |
Autosomal recessive hereditary disorder |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Associated morphology |
Congenital hyperplasia |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Finding site |
Entire endocrine gonad (body structure) |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Occurrence |
Congenital |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Finding site |
Adrenal cortex structure |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Is a |
Congenital anomaly of trunk |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Is a |
Virilizing syndrome of adrenal origin |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Is a |
Disorder of steroid metabolism |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Associated morphology |
Congenital hyperplasia |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Finding site |
Adrenal cortex structure |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Occurrence |
Congenital |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Associated morphology |
Hyperplasia |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Finding site |
Adrenal cortex structure |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Finding site |
Adrenal cortex structure |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Due to |
21-hydroxylase deficiency |
false |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Is a |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Due to |
Deficiency of steroid 21-monooxygenase |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Pathological process (attribute) |
Pathological developmental process (qualifier value) |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|
Steroid 21-monooxygenase deficiency, simple virilizing type |
Associated morphology |
Hyperplasia |
true |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
|