loading...| Preferred Name |
Congenital corneal dystrophy |
|
| Synonyms |
Congenital dystrophy of cornea Congenital dystrophy of cornea (disorder) |
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| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/1003408005 |
|
| Active |
1 |
|
| altLabel |
Congenital dystrophy of cornea Congenital dystrophy of cornea (disorder) |
|
| CASE SIGNIFICANCE ID |
900000000000448009 |
|
| CTV3ID |
XVESR |
|
| cui |
C1611195 |
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| DEFINITION STATUS ID |
900000000000073002 |
|
| Effective time |
20210131 |
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| Has associated morphology | ||
| Has finding site | ||
| Has pathological process | ||
| notation |
1003408005 |
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| Occurs in | ||
| prefLabel |
Congenital corneal dystrophy |
|
| Subset member |
6011000124106~MAPADVICE~IF CONGENITAL HEREDITARY ENDOTHELIAL DYSTROPHY AND PERCEPTIVE DEAFNESS SYNDROME CHOOSE H90.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 715484003 | Ophthalmomandibulomelic dysplasia | 447562003~MAPADVICE~ALWAYS H18.5 447562003~MAPRULE~TRUE 6011000124106~MAPRULE~IFA 95488001 | Congenital macular corneal dystrophy | 6011000124106~MAPPRIORITY~7 6011000124106~MAPPRIORITY~4 6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA 6011000124106~MAPTARGET~Q87.0 6011000124106~MAPTARGET~ 6011000124106~MAPCATEGORYID~447638001 6011000124106~MAPTARGET~H18.559 6011000124106~MAPGROUP~1 6011000124106~MAPGROUP~2 6011000124106~MAPADVICE~IF CONGENITAL LABIOSCROTAL AGENESIS, CEREBELLAR MALFORMATION, CORNEAL DYSTROPHY, FACIAL DYSMORPHISM SYNDROME CHOOSE Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 1172594000 | Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome | AND IFA 248153007 | Male (finding) | 6011000124106~MAPTARGET~H18.599 6011000124106~MAPPRIORITY~10 6011000124106~MAPADVICE~IF FRANCOIS SYNDROME CHOOSE H18.599 | CONSIDER LATERALITY SPECIFICATION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 231933003 | Lattice corneal dystrophy, isolated form | 6011000124106~MAPPRIORITY~8 6011000124106~MAPADVICE~IF FRANCOIS SYNDROME CHOOSE Q87.89 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF OPHTHALMOMANDIBULOMELIC DYSPLASIA CHOOSE H18.509 | CONSIDER LATERALITY SPECIFICATION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000508004~ACCEPTABILITYID~900000000000549004 6011000124106~MAPADVICE~IF STERN LUBINSKY DURRIE SYNDROME CHOOSE Q87.89 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF OPHTHALMOMANDIBULOMELIC DYSPLASIA CHOOSE Q74.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPGROUP~1 6011000124106~MAPTARGET~Q87.89 6011000124106~MAPRULE~IFA 254150007 | Francois syndrome | 447562003~CORRELATIONID~447561005 6011000124106~MAPCATEGORYID~447637006 6011000124106~MAPRULE~IFA 723584003 | Stern Lubinsky Durrie syndrome | 900000000000509007~ACCEPTABILITYID~900000000000548007 6011000124106~MAPADVICE~ALWAYS H18.509 | CONSIDER LATERALITY SPECIFICATION 900000000000508004~ACCEPTABILITYID~900000000000548007 447562003~MAPPRIORITY~1 6011000124106~MAPADVICE~IF CONGENITAL HEREDITARY ENDOTHELIAL DYSTROPHY AND PERCEPTIVE DEAFNESS SYNDROME CHOOSE H18.519 | CONSIDER LATERALITY SPECIFICATION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~Q04.9 447562003~MAPCATEGORYID~447637006 6011000124106~MAPADVICE~IF CONGENITAL LABIOSCROTAL AGENESIS, CEREBELLAR MALFORMATION, CORNEAL DYSTROPHY, FACIAL DYSMORPHISM SYNDROME CHOOSE H18.509 | CONSIDER LATERALITY SPECIFICATION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~H18.509 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPPRIORITY~5 6011000124106~MAPGROUP~4 6011000124106~MAPADVICE~IF CONGENITAL LABIOSCROTAL AGENESIS, CEREBELLAR MALFORMATION, CORNEAL DYSTROPHY, FACIAL DYSMORPHISM SYNDROME AND IF FEMALE CHOOSE Q52.71 | MAP IS CONTEXT DEPENDENT FOR GENDER 6011000124106~MAPADVICE~IF OPHTHALMOMANDIBULOMELIC DYSPLASIA CHOOSE Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~9 6011000124106~MAPCATEGORYID~447639009 6011000124106~MAPTARGET~H18.549 6011000124106~MAPADVICE~IF CONGENITAL LABIOSCROTAL AGENESIS, CEREBELLAR MALFORMATION, CORNEAL DYSTROPHY, FACIAL DYSMORPHISM SYNDROME AND IF MALE CHOOSE Q55.29 | MAP IS CONTEXT DEPENDENT FOR GENDER 6011000124106~MAPADVICE~IF CONGENITAL MACULAR CORNEAL DYSTROPHY CHOOSE H18.559 | CONSIDER LATERALITY SPECIFICATION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000497000~MAPTARGET~XVESR 6011000124106~MAPRULE~IFA 1172594000 | Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome | AND IFA 248152002 | Female (finding) | 6011000124106~MAPADVICE~IF LATTICE CORNEAL DYSTROPHY, ISOLATED FORM CHOOSE H18.549 | CONSIDER LATERALITY SPECIFICATION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF CONGENITAL LABIOSCROTAL AGENESIS, CEREBELLAR MALFORMATION, CORNEAL DYSTROPHY, FACIAL DYSMORPHISM SYNDROME CHOOSE Q04.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~1 6011000124106~MAPTARGET~Q55.29 6011000124106~MAPPRIORITY~6 6011000124106~CORRELATIONID~447561005 6011000124106~MAPTARGET~Q74.8 6011000124106~MAPGROUP~3 6011000124106~MAPPRIORITY~3 900000000000509007~ACCEPTABILITYID~900000000000549004 6011000124106~MAPTARGET~H18.519 6011000124106~MAPPRIORITY~2 6011000124106~MAPTARGET~H90.5 6011000124106~MAPRULE~IFA 720749004 | Congenital hereditary endothelial dystrophy and perceptive deafness syndrome | 6011000124106~MAPTARGET~Q52.71 447562003~MAPTARGET~H18.5 6011000124106~MAPRULE~IFA 1172594000 | Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome | |
|
| tui |
T019 |
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| Type ID |
900000000000003001 900000000000013009 |
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| subClassOf |