Disease #03132 (APL (leukemia, acute, promyelocytic), OMIM:612376)

Official abbreviation APL
Name leukemia, acute, promyelocytic
OMIM ID 612376
Human Phenotype Ontology Project (HPO) HPO
Inheritance Somatic mosaicism
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 2 genes NUMA1, RARA
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2026-04-28 14:26:46 +02:00 (CEST)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00034561 - - - F - - European, white - - - - APL promyelocytic leukaemia NRAS NRAS 1 1 Phil Chambers
00478081 Pat1 PubMed: Astofi 2021 - F - Italy - - - - - APL see paper; ... RARA RARA 1 1 Johan den Dunnen
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