loading...| Preferred Name |
Endemic cretinism |
|
| Synonyms |
Endemic cretinism (disorder) |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/75065003 |
|
| Active |
1 |
|
| altLabel |
Endemic cretinism (disorder) |
|
| Associated finding of | ||
| CASE SIGNIFICANCE ID |
900000000000020002 900000000000448009 900000000000017005 |
|
| CTV3ID |
X40I6 |
|
| cui |
C0342200 |
|
| DEFINITION STATUS ID |
900000000000073002 |
|
| Effective time |
20210930 |
|
| Has associated morphology | ||
| Has finding site | ||
| Has pathological process | ||
| INACTIVATION INDICATOR |
900000000000485001 900000000000494007 |
|
| notation |
75065003 |
|
| Occurs in | ||
| prefLabel |
Endemic cretinism |
|
| Subset member |
447562003~MAPRULE~TRUE 447562003~MAPRULE~IFA 237565000 | Congenital iodine deficiency syndrome - mixed type (disorder) | 6011000124106~MAPTARGET~E00.2 447562003~MAPTARGET~E00.0 447562003~MAPADVICE~IF CONGENITAL IODINE DEFICIENCY SYNDROME - NEUROLOGICAL TYPE CHOOSE E00.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~E00.9 6011000124106~MAPADVICE~IF CONGENITAL IODINE DEFICIENCY SYNDROME - MIXED TYPE CHOOSE E00.2 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~4 900000000000490003~VALUEID~900000000000494007 6011000124106~MAPADVICE~IF CONGENITAL IODINE DEFICIENCY SYNDROME OF NEUROLOGICAL TYPE CHOOSE E00.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 440092001 | Endemic congenital iodine deficiency syndrome of myxedematous type (disorder) | 6011000124106~MAPRULE~IFA 237565000 | Congenital iodine deficiency syndrome - mixed type (disorder) | 6011000124106~MAPGROUP~1 6011000124106~MAPRULE~IFA 237566004 | Congenital iodine deficiency syndrome - neurological type | 447562003~MAPTARGET~E00.1 6011000124106~MAPADVICE~IF CONGENITAL IODINE DEFICIENCY SYNDROME - NEUROLOGICAL TYPE CHOOSE E00.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~E00.1 900000000000508004~ACCEPTABILITYID~900000000000549004 6011000124106~MAPADVICE~IF CONGENITAL IODINE DEFICIENCY SYNDROME OF MIXED TYPE CHOOSE E00.2 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF ENDEMIC CONGENITAL IODINE DEFICIENCY SYNDROME OF MYXEDEMATOUS TYPE CHOOSE E00.1 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000531004~TARGETCOMPONENT~440092001 447562003~MAPGROUP~1 447562003~CORRELATIONID~447561005 447562003~MAPRULE~OTHERWISE TRUE 900000000000497000~MAPTARGET~X40I6 6011000124106~MAPCATEGORYID~447637006 900000000000509007~ACCEPTABILITYID~900000000000548007 6011000124106~MAPRULE~IFA 440092001 | Endemic congenital iodine deficiency syndrome of myxedematous type | 6011000124106~MAPRULE~IFA 237565000 | Congenital iodine deficiency syndrome - mixed type | 900000000000508004~ACCEPTABILITYID~900000000000548007 6011000124106~MAPRULE~IFA 237566004 | Congenital iodine deficiency syndrome of neurological type | 447562003~MAPTARGET~E00.9 900000000000490003~VALUEID~900000000000485001 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 6011000124106~MAPRULE~OTHERWISE TRUE 900000000000531004~TARGETCOMPONENT~217710005 6011000124106~MAPTARGET~E00.0 6011000124106~MAPCATEGORYID~447639009 447562003~MAPADVICE~IF CONGENITAL IODINE DEFICIENCY SYNDROME - MIXED TYPE CHOOSE E00.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPPRIORITY~3 447562003~MAPCATEGORYID~447639009 6011000124106~MAPPRIORITY~1 447562003~MAPTARGET~E00.2 447562003~MAPADVICE~ALWAYS E00.9 6011000124106~MAPRULE~IFA 237566004 | Congenital iodine deficiency syndrome - neurological type (disorder) | 6011000124106~CORRELATIONID~447561005 6011000124106~MAPRULE~IFA 237565000 | Congenital iodine deficiency syndrome of mixed type | 447562003~MAPRULE~IFA 440092001 | Endemic congenital iodine deficiency syndrome of myxedematous type (disorder) | 447562003~MAPPRIORITY~2 6011000124106~MAPADVICE~ALWAYS E00.9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE 900000000000531004~TARGETCOMPONENT~190268003 6011000124106~MAPPRIORITY~3 900000000000509007~ACCEPTABILITYID~900000000000549004 6011000124106~MAPPRIORITY~2 447562003~MAPADVICE~IF ENDEMIC CONGENITAL IODINE DEFICIENCY SYNDROME OF MYXEDEMATOUS TYPE CHOOSE E00.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPRULE~IFA 237566004 | Congenital iodine deficiency syndrome - neurological type (disorder) | 447562003~MAPPRIORITY~4 |
|
| tui |
T047 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |