MOLPATH.DEL   LP7823-0

LOINC Hierarchy


LOINC part codeLP7823-0
nameMOLPATH.DEL
typeCLASS
statusACTIVE
children
LOINC Home
   {component}   LP432695-7
      Laboratory   LP29693-6
         Molecular pathology   LP7822-2
            Genetic screen   LP19405-7
               Deletions   LP7823-0

Fetal Prader-Willi syndrome risk   LP185770-7

Prader-Willi syndrome prior risk   LP185769-9

Comment on fetal Prader-Willi syndrome risk   LP185992-7

1p chromosome   LP36880-0

1p and 19q chromosome   LP36171-4

Fetal 1p36 deletion risk   LP185774-9

1p36 deletion prior risk   LP185773-1

Comment on fetal 1p36 deletion risk   LP185994-3

Fetal 5p deletion risk   LP185908-3

5p deletion prior risk   LP186095-8

Comment on fetal 5p deletion risk   LP185993-5

5p15.2 chromosome deletion   LP227508-1

9p21 chromosome   LP97916-8

9q34 chromosome region   LP189751-3

18q chromosome   LP40277-3

19q chromosome   LP36881-8

20q chromosome   LP70661-1

Fetal 22q11.2 deletion risk   LP185776-4

22q11.2 deletion prior risk   LP185768-1

Comment on fetal 22q11.2 deletion risk   LP185989-3

Y chromosome   LP33230-1


Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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