Steroid 21-monooxygenase deficiency, simple virilizing type 52604008

SNOMED CT code

SNOMED code

52604008

name

Steroid 21-monooxygenase deficiency, simple virilizing type

status

active

date introduced

2002-01-31

fully specified name(s)

Steroid 21-monooxygenase deficiency, simple virilizing type (disorder)

synonyms

Steroid 21-hydroxylase deficiency, simple virilising type
Steroid 21-hydroxylase deficiency, simple virilizing type
Steroid 21-monooxygenase deficiency, simple virilising type
Simple-virilising congenital adrenal hyperplasia
Simple virilising adrenal hyperplasia
Simple-virilizing congenital adrenal hyperplasia
Steroid 21-monooxygenase deficiency, simple virilizing type
Simple virilizing adrenal hyperplasia
Adrenogenital disorder due to 21-hydroxylase deficiency
Congenital adrenal hyperplasia, type 1

attributes - group1

Pathological process

Pathological developmental process 308490002

Associated morphology

Hyperplasia 76197007

Occurrence

Congenital 255399007

Finding site

Adrenal cortex structure 68594002

attributes - group2

Due to

Deficiency of steroid 21-monooxygenase 124221007

parents

Virilizing syndrome of adrenal origin 17318002
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 717261006

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Viscus structure finding 406123005
Abdominal organ finding 249561001
Disorder of adrenal gland 30171000
Adrenogenital disorder 267395000
Virilizing syndrome of adrenal origin 17318002
Steroid 21-monooxygenase deficiency, simple virilizing type 52604008

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Congenital adrenal hyperplasia 237751000
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 717261006
Steroid 21-monooxygenase deficiency, simple virilizing type 52604008

ancestors

sorted most to least specific

Virilizing syndrome of adrenal origin 17318002
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 717261006
Congenital adrenal hyperplasia 237751000
Adrenogenital disorder 267395000
Adrenocortical hyperplasia 237777008
Developmental hereditary disorder 363070008
Hereditary disorder of endocrine system 363104002
Congenital anomaly of adrenal gland 60637003
Autosomal recessive hereditary disorder 85995004
Disorder of adrenal cortex 129636003
Autosomal hereditary disorder 1899006
Adrenal hyperplasia 419920004
Hereditary disorder by system 363137000
Congenital anomaly of abdomen 363024001
Congenital anomaly of endocrine gland 4184009
Disorder of adrenal gland 30171000
Hereditary disease 32895009
Congenital anomaly of lower trunk 363030001
Abdominal organ finding 249561001
Disorder of endocrine system 362969004
Disorder of retroperitoneum 734045002
Genetic disease 782964007
Congenital abnormality of lower limb and pelvic girdle 253937004
Congenital anomaly of trunk 78626001
Viscus structure finding 406123005
Disorder of body system 362965005
Disorder of abdomen 118948005
Congenital malformation 276654001
Finding of abdomen 609624008
Disorder of abdominopelvic segment of trunk 822988000
Developmental disorder 5294002
Congenital disease 66091009
Finding of abdominopelvic segment of trunk 822987005
Disorder of trunk 128121009
Disease 64572001
Finding of trunk structure 302292003
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Viscus structure finding 406123005

Abdominal organ finding 249561001

Disorder of adrenal gland 30171000

Adrenogenital disorder 267395000

Virilizing syndrome of adrenal origin 17318002

Steroid 21-monooxygenase deficiency, simple virilizing type 52604008

SNOMED CT code