75585-0  Genetic counselor comment on fetal Prader-Willi syndrome risk [Text] in Plasma cell-free+​WBC DNA by Dosage of chromosome-specific cfDNA NarrativeGenetic counselor comment on fetal Prader-Willi syndrome risk [Text] in Plasma cell-free+​WBC DNA by Dosage of chromosome-specific cfDNA NarrativeGenetic counselor comment on fetal Prader-Willi syndrome risk: Txt: Pt: WBC.DNA+​Plas.cfDNA: Nar: Dosage of chromosome specific cf DNA  

NAME
  Fully Specified Name: 
Component   Property   Time   System   Scale   Method
Genetic counselor comment on fetal Prader-Willi syndrome risk  Txt  Pt  WBC.DNA+Plas.cfDNA  Nar  Dosage of chromosome specific cf DNA
  Long Common Name:  Genetic counselor comment on fetal Prader-Willi syndrome risk [Text] in Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA Narrative
  Short Name:  Gen couns comm Fet PWS risk
  Display Name:  Genetic counselor comment on Prader-Willi syndrome 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.
 
 

PART DEFINITION/DESCRIPTION(S)
  Part: Genetic counselor comment on fetal Prader-Willi syndrome risk
  The genetic counselor's comment regarding risk of a specific disorder or group of disorders is used to convey follow-up recommendations or other information related to the risk result and interpretation.
 
 
  Part: Genetic counselor comment on fetal Prader-Willi syndrome risk
  Prader-Willi syndrome (PWS) risk refers to the fetus's risk of being affected by PWS. The risk for the fetus can be derived from the general population risk as well as prenatal genetic testing of fetal DNA. PWS is caused by the functional loss of several genes on chromosome 15. Normally, only the paternal copy of these genes is active due to genomic imprinting, and in PWS, the paternal copy of these genes is missing. The genetic basis for PWS is the inverse of the basis for Angelman syndrome, in which the maternal copy of a specific gene on chromosome 15 is missing. About 70% of PWS cases are due to the deletion of a portion of the paternal chromosome 15, and another 25% are due to the presence of two maternal chromosome 15 copies (called uniparental disomy, meaning two copies from one parent) instead of one maternal and one paternal.
PWS is associated with different characteristics over time. Infants with PWS have poor growth, developmental delay, and weak muscle tone. Children with PWS develop a compulsion to eat, which leads to obesity and type 2 diabetes mellitus. PWS is associated with mild to moderate cognitive delay, behavior problems, characteristic facial features, and delayed puberty. The general population risk of PWS is about 1 in 10,000 - 30,000 live births, and does not change with maternal age. [GHR: prader-willi-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   LP185992-7  Genetic counselor comment on fetal Prader-Willi syndrome risk 
Property   LP6885-0  Txt   [Text] 
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   LP20987-1  Comment 
Fragments for synonyms   LP247965-9  Genetic 
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))
 
  Genetic counselor comment on Prader-Willi syndrome risk:Txt:Pt:WBC.DNA+​Plas.cfDNA:Nar:Dosage of chromosome specific cf DNAGenetic counselor comment on Prader-Willi syndrome risk:Txt:Pt:WBC.DNA+​Plas.cfDNA:Nar:Dosage of chromosome specific cf DNARisque syndrome de Prader-Willi commentaire du conseiller génétique [Texte] Leucocytes ADN+​Plasma avec ADN libre circulant ; Résultat textuel ; Dosage d'ADN libre circulant spécifiques aux chromosomes

RELATED NAMES
  Chromosom Genomic PWS risk
  Chromosomes Leukocytes Random
  cmmt Molecular pathology Remarks
  cmnt MOLPATH Report
  Com MOLPATH.DELETIONS Spec
  Comm Narrative Text
  Comments Pl WBC.DNA+cfDNA
  Commt Plasma WBCs
  Gen couns comm fet PWS risk Plsm White blood cells
  Genetics Point in time  

CHANGE HISTORY
  Change Type: NAM

INTERNAL FIELDS
  Detail Page Created On: 6/26/2019 2:43:16 PM
  Long Common Name: Genetic counselor comment on fetal Prader-Willi syndrome risk [Text] in Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA Narrative
  Shortname: Gen couns comm Fet PWS risk
  Fully Specified Name: Genetic counselor comment on fetal Prader-Willi syndrome risk: Txt: Pt: WBC.DNA+Plas.cfDNA: Nar: Dosage of chromosome specific cf DNA
     
  Component Word Count: 9
  ID: 77273
  Status (Raw): ACTIVE