MOLPATH.DEL LP7823-0
LOINC Hierarchy
| LOINC part code | LP7823-0 |
|---|---|
| name | MOLPATH.DEL |
| type | CLASS |
| status | ACTIVE |
| 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 © 2026 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2026, 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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