75601-5  Fetal 1p36 deletion risk [Likelihood] based on Plasma cell-free+​WBC DNA by Dosage of chromosome-specific cfDNA NarrativeFetal 1p36 deletion risk [Likelihood] based on Plasma cell-free+​WBC DNA by Dosage of chromosome-specific cfDNA NarrativeFetal 1p36 deletion risk: Likelihood: Pt: WBC.DNA+​Plas.cfDNA: Nar: Dosage of chromosome specific cf DNA  

NAME
  Fully Specified Name: 
Component   Property   Time   System   Scale   Method
Fetal 1p36 deletion risk  Likelihood  Pt  WBC.DNA+Plas.cfDNA  Nar  Dosage of chromosome specific cf DNA
  Long Common Name:  Fetal 1p36 deletion risk [Likelihood] based on Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA Narrative
  Short Name:  Fet 1p36 del risk WBC.DNA+cfDNA
  Display Name:  1p36 del risk Dosage of chromosome-specific cfDNA Nar (Plasma cell-free+WBC DNA)

TERM DEFINITION/DESCRIPTION(S)
  This term was developed for, but is not limited in use to, Natera's Panorama noninvasive prenatal test for fetal aneuploidies and microdeletions. It represents the risk based on a priori risk combined with the Panorama test result.
 
 

PART DEFINITION/DESCRIPTION(S)
  Part: Fetal 1p36 deletion risk
  1p36 deletion syndrome is caused by the deletion of several genes in the short arm of chromosome 1 and is associated with severe cognitive delay, seizure disorder, weak muscle tone, swallowing difficulty, and distinctive facial features. The general population risk of 1p36 deletion is about 1 in 5,000 - 10,000 live births, and does not change with maternal age. Fetal risk of having 1p36 deletion syndrome can be derived from the general population risk as well as prenatal genetic testing of fetal DNA. [GHR: 1p36-deletion-syndrome]
 
 

BASIC ATTRIBUTES
  Class/Type: MOLPATH.DEL/Lab
  Common Lab Results Rank: #3000
  Common SI Lab Results Rank: #3000
  First Released in Version: 2.50
  Last Updated in Version: 2.66
  Order vs. Obs.: Both
  Status: Active.
Change Reason: Added "Fetal" to Component to clarify that the result is about the fetus.

MEMBER OF THESE PANELS     
  This section provides information about panels that contain this LOINC code.
  LOINC   Long Common Name  
  75547-0 Noninvasive prenatal fetal aneuploidy and microdeletion panel based on Plasma cell-free+WBC DNA by Dosage of chromosome-specific circulating cell free (ccf) DNA
  

PARTS

Part Type    Part No.  Part Name   
Component   LP185774-9  Fetal 1p36 deletion risk 
Property   LP185777-2  Likelihood 
Time   LP6960-1  Pt   [Point in time (spot)] 
System   LP185797-0  WBC.DNA+Plas.cfDNA   [Plasma cell-free+WBC DNA] 
Scale   LP7749-7  Nar 
Method   LP172871-8  Dosage of chromosome specific cf DNA   [Dosage of chromosome-specific cfDNA] 
Fragments for synonyms   LP20948-3  Chromosome 
Fragments for synonyms   LP28586-3  Specific 

LANGUAGE VARIANTS
  French (FRANCE)  (From: ASIP Santé (Agence des systèmes d'information partagés de santé))
 
  1p36 deletion risk:Likelihood:Pt:WBC.DNA+​Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA1p36 deletion risk:Likelihood:Pt:WBC.DNA+​Plas.cfDNA:Nar:Dosage of chromosome specific cf DNARisque délétion 1p36 [Probabilité] Leucocytes ADN+​Plasma avec ADN libre circulant ; Résultat textuel ; Dosage d'ADN libre circulant spécifiques aux chromosomes

RELATED NAMES
  1p36 del risk Narrative Risk
  Chromosom Pl Spec
  Chromosomes Plasma WBC.DNA+cfDNA
  Leukocytes Plsm WBCs
  Molecular pathology Point in time White blood cells
  MOLPATH Random  
  MOLPATH.DELETIONS Report  

CHANGE HISTORY
  Change Type: NAM

INTERNAL FIELDS
  Detail Page Created On: 6/26/2019 2:43:15 PM
  Long Common Name: Fetal 1p36 deletion risk [Likelihood] based on Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA Narrative
  Shortname: Fet 1p36 del risk WBC.DNA+cfDNA
  Fully Specified Name: Fetal 1p36 deletion risk: Likelihood: Pt: WBC.DNA+Plas.cfDNA: Nar: Dosage of chromosome specific cf DNA
     
  Component Word Count: 4
  ID: 77289
  Status (Raw): ACTIVE