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SNOMED CT
| Id | http://purl.bioontology.org/ontology/SNOMEDCT/763792009
http://purl.bioontology.org/ontology/SNOMEDCT/763792009
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|---|---|
| Preferred Name | Leukonychia totalis |
| Definitions |
A rare nail anomaly disorder characterized by complete white discoloration of the nails. Patients typically present white, chalky nails as an isolated finding, although other cutaneous or systemic manifestations could also be present. There is evidence the disease can be caused by homozygous or heterozygous mutation in the PLCD1 gene on chromosome 3p22-p21.3.
A rare nail anomaly disorder characterised by complete white discolouration of the nails. Patients typically present white, chalky nails as an isolated finding, although other cutaneous or systemic manifestations could also be present. There is evidence the disease can be caused by homozygous or heterozygous mutation in the PLCD1 gene on chromosome 3p22-p21.3.
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| Synonyms |
Leukonychia totalis (disorder)
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | A rare nail anomaly disorder characterized by complete white discoloration of the nails. Patients typically present white, chalky nails as an isolated finding, although other cutaneous or systemic manifestations could also be present. There is evidence the disease can be caused by homozygous or heterozygous mutation in the PLCD1 gene on chromosome 3p22-p21.3. A rare nail anomaly disorder characterized by complete white discoloration of the nails. Patients typically present white, chalky nails as an isolated finding, although other cutaneous or systemic manifestations could also be present. There is evidence the disease can be caused by homozygous or heterozygous mutation in the PLCD1 gene on chromosome 3p22-p21.3. A rare nail anomaly disorder characterised by complete white discolouration of the nails. Patients typically present white, chalky nails as an isolated finding, although other cutaneous or systemic manifestations could also be present. There is evidence the disease can be caused by homozygous or heterozygous mutation in the PLCD1 gene on chromosome 3p22-p21.3. |
|---|---|
| altLabel | Leukonychia totalis (disorder)
|
| prefLabel | Leukonychia totalis
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| Type ID |
900000000000003001
900000000000013009
|
| CASE SIGNIFICANCE ID | 900000000000448009
|
| notation | 763792009
|
| Effective time | 20180731
|
| Active | 1
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| Has finding site | |
| interprets | |
| Has pathological process | |
| subClassOf | |
| Semantic type UMLS property | |
| type | |
| Subset member | 447562003~MAPRULE~TRUE
447562003~MAPADVICE~ALWAYS Q84.4
6011000124106~MAPTARGET~Q84.4
6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
6011000124106~MAPTARGET~
6011000124106~MAPCATEGORYID~447638001
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
6011000124106~MAPRULE~IFA 774065001 | FLOTCH syndrome |
6011000124106~MAPADVICE~ALWAYS Q84.4
447562003~MAPGROUP~1
6011000124106~MAPTARGET~Q82.8
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~IF LEUKONYCHIA TOTALIS, ACANTHOSIS-NIGRICANS-LIKE LESIONS, ABNORMAL HAIR SYNDROME CHOOSE Q84.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
900000000000497000~MAPTARGET~XV1xE
900000000000508004~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~IF FLOTCH SYNDROME CHOOSE L72.12 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
6011000124106~MAPRULE~IFA 773700005 | Leukonychia totalis, acanthosis-nigricans-like lesions, abnormal hair syndrome |
447562003~MAPTARGET~Q84.4
6011000124106~MAPRULE~OTHERWISE TRUE
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPTARGET~Q84.2
6011000124106~MAPADVICE~IF LEUKONYCHIA TOTALIS, ACANTHOSIS-NIGRICANS-LIKE LESIONS, ABNORMAL HAIR SYNDROME CHOOSE Q82.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~L72.12
6011000124106~MAPADVICE~IF FLOTCH SYNDROME CHOOSE Q84.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
6011000124106~MAPRULE~TRUE
6011000124106~MAPGROUP~3
6011000124106~MAPPRIORITY~3
6011000124106~MAPPRIORITY~2
6011000124106~MAPADVICE~IF LEUKONYCHIA TOTALIS, ACANTHOSIS-NIGRICANS-LIKE LESIONS, ABNORMAL HAIR SYNDROME CHOOSE Q84.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
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| DEFINITION STATUS ID | 900000000000074008
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| tui | T033
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| CTV3ID | XV1xE
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| Occurs in | |
| cui | C4551625
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| Has associated morphology |
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| No notes to display |