loading...| Preferred Name |
Nephrocalcinosis |
|
| Synonyms |
Nephrocalcinosis (disorder) |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/48638002 |
|
| Active |
1 |
|
| altLabel |
Nephrocalcinosis (disorder) |
|
| CASE SIGNIFICANCE ID |
900000000000448009 |
|
| CTV3ID |
C3547 |
|
| cui |
C0027709 |
|
| DEFINITION STATUS ID |
900000000000074008 |
|
| Effective time |
20020131 |
|
| Has associated morphology | ||
| Has finding site | ||
| notation |
48638002 |
|
| prefLabel |
Nephrocalcinosis |
|
| Subset member |
6011000124106~MAPADVICE~IF ENAMEL-RENAL SYNDROME CHOOSE K00.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~E83.52 447562003~MAPRULE~TRUE 447562003~MAPRULE~IFA 700112007 | Bartter syndrome type 4 (disorder) | 6011000124106~MAPTARGET~E83.59 447562003~MAPTARGET~E26.8 6011000124106~MAPPRIORITY~4 447562003~MAPADVICE~IF BARTTER SYNDROME ANTENATAL TYPE 1 CHOOSE E26.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA 6011000124106~MAPRULE~IFA 725033008 | Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement | AND IFA 445518008 | Age at onset of clinical finding (observable entity) | < 29.0 days 6011000124106~MAPADVICE~IF FAMILIAL PRIMARY HYPOMAGNESEMIA WITH HYPERCALCIURIA AND NEPHROCALCINOSIS WITHOUT SEVERE OCULAR INVOLVEMENT CHOOSE E83.42 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~ 6011000124106~MAPCATEGORYID~447638001 6011000124106~MAPADVICE~ALWAYS N29 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE 6011000124106~MAPADVICE~IF FAMILIAL PRIMARY HYPOMAGNESEMIA WITH HYPERCALCIURIA AND NEPHROCALCINOSIS WITHOUT SEVERE OCULAR INVOLVEMENT CHOOSE N29 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPGROUP~1 6011000124106~MAPGROUP~2 447562003~MAPGROUP~2 447562003~MAPRULE~IFA 236445002 | Macroscopic nephrocalcinosis (disorder) | 6011000124106~MAPRULE~IFA 59531002 | Tryptophan malabsorption syndrome | 447562003~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA 447562003~MAPADVICE~IF MICROSCOPIC NEPHROCALCINOSIS CHOOSE N29.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPRULE~IFA 276584001 | Neonatal nephrocalcinosis (disorder) | 447562003~MAPPRIORITY~5 447562003~MAPGROUP~1 447562003~CORRELATIONID~447561005 6011000124106~MAPADVICE~ALWAYS E83.59 447562003~MAPRULE~OTHERWISE TRUE 6011000124106~MAPADVICE~IF ENAMEL-RENAL SYNDROME CHOOSE N29 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPCATEGORYID~447637006 447562003~MAPRULE~IFA 700107006 | Bartter syndrome antenatal type 1 (disorder) | 900000000000509007~ACCEPTABILITYID~900000000000548007 6011000124106~MAPADVICE~IF FAMILIAL PRIMARY HYPOMAGNESEMIA WITH HYPERCALCIURIA AND NEPHROCALCINOSIS WITHOUT SEVERE OCULAR INVOLVEMENT AND IF AGE AT ONSET OF CLINICAL FINDING BEFORE 29.0 DAYS CHOOSE P71.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPTARGET~E70.8 447562003~MAPRULE~IFA 700109009 | Bartter syndrome antenatal type 2 (disorder) | 447562003~MAPRULE~IFA 59531002 | Tryptophan malabsorption syndrome (disorder) | 900000000000508004~ACCEPTABILITYID~900000000000548007 447562003~MAPTARGET~ 900000000000497000~MAPTARGET~C3547 447562003~MAPPRIORITY~1 447562003~MAPADVICE~IF BARTTER SYNDROME TYPE 4 CHOOSE E26.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPCATEGORYID~447637006 447562003~MAPTARGET~N29.8 6011000124106~MAPRULE~IFA 109477002 | Enamel-renal syndrome | 447562003~MAPRULE~IFA 236444003 | Microscopic nephrocalcinosis (disorder) | 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPPRIORITY~5 6011000124106~MAPADVICE~ALWAYS E83.59 | DESCENDANTS NOT EXHAUSTIVELY MAPPED 6011000124106~MAPCATEGORYID~447639009 6011000124106~MAPRULE~IFA 725033008 | Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement | 447562003~MAPADVICE~IF NEONATAL NEPHROCALCINOSIS CHOOSE P96.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPPRIORITY~3 447562003~MAPTARGET~P96.8 6011000124106~MAPADVICE~IF TRYPTOPHAN MALABSORPTION SYNDROME CHOOSE E72.09 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPCATEGORYID~447639009 6011000124106~MAPPRIORITY~1 447562003~MAPADVICE~IF BARTTER SYNDROME ANTENATAL TYPE 2 CHOOSE E26.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~CORRELATIONID~447561005 447562003~MAPADVICE~IF TRYPTOPHAN MALABSORPTION SYNDROME CHOOSE E70.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF FAMILIAL PRIMARY HYPOMAGNESEMIA WITH HYPERCALCIURIA AND NEPHROCALCINOSIS WITHOUT SEVERE OCULAR INVOLVEMENT CHOOSE E83.52 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~E83.42 447562003~MAPPRIORITY~2 6011000124106~MAPRULE~TRUE 6011000124106~MAPGROUP~3 6011000124106~MAPPRIORITY~3 6011000124106~MAPTARGET~N29 6011000124106~MAPPRIORITY~2 6011000124106~MAPTARGET~E72.09 447562003~MAPADVICE~IF MACROSCOPIC NEPHROCALCINOSIS CHOOSE N29.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPTARGET~E83.5 6011000124106~MAPADVICE~ALWAYS N29 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | DESCENDANTS NOT EXHAUSTIVELY MAPPED 6011000124106~MAPTARGET~K00.5 6011000124106~MAPTARGET~P71.2 447562003~MAPCATEGORYID~447638001 447562003~MAPADVICE~ALWAYS E83.5 447562003~MAPPRIORITY~4 |
|
| tui |
T047 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |
http://purl.bioontology.org/ontology/SNOMEDCT/79131000119100 http://purl.bioontology.org/ontology/SNOMEDCT/6595006 |