Deletions LP7823-0
LOINC Hierarchy
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▸ 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 © 2023 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2023, 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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