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Logical Observation Identifier Names and Codes
Last uploaded:
January 16, 2025
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| Id | http://purl.bioontology.org/ontology/LNC/82238-7
http://purl.bioontology.org/ontology/LNC/82238-7
|
|---|---|
| Preferred Name | Chromosome region 15q11-13 deletion+duplication:Find:Pt:Amnio fld/CVS:Doc:FISH |
| Synonyms |
Chromosome region 15q11-13 deletion+duplication:Finding:To identify measures at a point in time:Amniotic fluid/CVS:Document:FISH
15q11-13 del and dup mutation analysis FISH Doc (Amnio fld/CVS)
Chr 15q11-13 Del+Dup Amn/CVS FISH
Chromosome region 15q11-13 deletion and duplication mutation analysis in Amniotic fluid or Chorionic villus sample by FISH
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel | Chromosome region 15q11-13 deletion+duplication:Finding:To identify measures at a point in time:Amniotic fluid/CVS:Document:FISH
15q11-13 del and dup mutation analysis FISH Doc (Amnio fld/CVS)
Chr 15q11-13 Del+Dup Amn/CVS FISH
Chromosome region 15q11-13 deletion and duplication mutation analysis in Amniotic fluid or Chorionic villus sample by FISH
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|---|---|
| prefLabel | Chromosome region 15q11-13 deletion+duplication:Find:Pt:Amnio fld/CVS:Doc:FISH
|
| LOINC time aspect | Pt
|
| VERSION LAST CHANGED | 2.65
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| notation | 82238-7
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| Has class | |
| Has property | |
| LOR | Both
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| COMMON ORDER RANK | 0
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| LOINC property | Find
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| LOINC system | Amnio fld/CVS
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| LCL | MOLPATH.DELDUP
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| VERSION FIRST RELEASED | 2.56
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| CONSUMER NAME | 15q11-13 deletion/duplication analysis, Amnio Fld/CVS
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| ASSOC OBSERVATIONS | 81247-9
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| Has scale | |
| Has component | |
| Has method | |
| Has system | |
| LCS | ACTIVE
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| Related names 2 | AF; Amn; Amn fl; Amn/CVS; Amnio; Amniotic flu; Amniotic fluid; Amplification; Angelman + Prader Willi syndrome; Angelman syndrome; AWS; Chorionic villi; Chorionic villus sample; Chr 15q11-13; Chr 15q11-13 deletion+duplication; Chromosom; Chromosomes; Cyto loc; Del; Del+Dup; Deletions; Document; Dp; Finding; Findings; Fluorescent in situ hybridization; Genetics; Gyn; Gynecology; Heredity; Heritable; Inherited; Molecular pathology; MOLPATH; MOLPATH.DELDUP; OB; ObGyn; Obstetrics; Point in time; Prader Willi syndrome; Random
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| LCT | MIN
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| LOINC scale type | Doc
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| subClassOf | |
| Semantic type UMLS property | |
| measures | |
| LOINC component | Chromosome region 15q11-13 deletion+duplication
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| Has suffix | |
| LOINC method type | FISH
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| type | |
| COMMON TEST RANK | 0
|
| LCN | 1
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| Has time aspect | |
| tui | T201
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| cui | C4264697
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| analyzes |
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