Steroid 21-monooxygenase deficiency, salt wasting type 71578002

SNOMED CT code

SNOMED code

71578002

name

Steroid 21-monooxygenase deficiency, salt wasting type

status

active

date introduced

2002-01-31

fully specified name(s)

Steroid 21-monooxygenase deficiency, salt wasting type (disorder)

synonyms

Steroid 21-monooxygenase deficiency, salt wasting type
Congenital adrenal hyperplasia, type 2
21-hydroxylase deficiency, salt wasting type

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

Salt-losing congenital adrenal hyperplasia 237753002
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 717261006

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Congenital adrenal hyperplasia 237751000
Salt-losing congenital adrenal hyperplasia 237753002
Steroid 21-monooxygenase deficiency, salt wasting type 71578002

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, salt wasting type 71578002

ancestors

sorted most to least specific

Salt-losing congenital adrenal hyperplasia 237753002
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 717261006
Congenital adrenal hyperplasia 237751000
Adrenocortical hyperplasia 237777008
Adrenogenital disorder 267395000
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
Genetic disease 782964007
Disorder of endocrine system 362969004
Disorder of retroperitoneum 734045002
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
Developmental disorder 5294002
Disorder of abdominopelvic segment of trunk 822988000
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

Disease 64572001

Developmental disorder 5294002

Developmental hereditary disorder 363070008

Congenital adrenal hyperplasia 237751000

Salt-losing congenital adrenal hyperplasia 237753002

Steroid 21-monooxygenase deficiency, salt wasting type 71578002

SNOMED CT code