Preferred Name |
Deficiency of steroid 17-alpha-monooxygenase |
|
Synonyms |
CAH - 17-alpha-hydroxysteroid dehydrogenase deficiency |
|
ID |
http://purl.bioontology.org/ontology/SNOMEDCT/124220008 |
|
Active |
1 |
|
altLabel |
CAH - 17-alpha-hydroxysteroid dehydrogenase deficiency 17 alpha-Hydroxylase deficiency Steroid 17-alpha-monooxygenase deficiency Adrenogenital disorder due to 17-alpha-hydroxylase deficiency Deficiency of steroid 17-alpha-monooxygenase (disorder) Deficiency of steroid 17-alpha-hydroxylase Congenital adrenal hyperplasia, type 5 CAH - 17-hydroxylase deficiency |
|
CASE SIGNIFICANCE ID |
900000000000448009 900000000000017005 |
|
CTV3ID |
C1526 |
|
cui |
C0268285 |
|
DEFINITION STATUS ID |
900000000000074008 |
|
Effective time |
20020131 |
|
Has associated morphology | ||
Has finding site | ||
Has pathological process | ||
notation |
124220008 |
|
Occurs in | ||
prefLabel |
Deficiency of steroid 17-alpha-monooxygenase |
|
Subset member |
447562003~MAPRULE~TRUE 6011000124106~MAPGROUP~1 900000000000508004~ACCEPTABILITYID~900000000000549004 447562003~MAPGROUP~1 447562003~CORRELATIONID~447561005 6011000124106~MAPCATEGORYID~447637006 447562003~MAPADVICE~ALWAYS E25.0 900000000000509007~ACCEPTABILITYID~900000000000548007 900000000000508004~ACCEPTABILITYID~900000000000548007 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 900000000000497000~MAPTARGET~C1526 6011000124106~MAPADVICE~ALWAYS E88.89 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE 6011000124106~MAPPRIORITY~1 447562003~MAPTARGET~E25.0 6011000124106~CORRELATIONID~447561005 6011000124106~MAPTARGET~E88.89 6011000124106~MAPRULE~TRUE 900000000000509007~ACCEPTABILITYID~900000000000549004 |
|
tui |
T047 |
|
Type ID |
900000000000003001 900000000000013009 |
|
subClassOf |