Disease #00167 (FANCM (Fanconi anemia, complementation group M), OMIM:614087)

Official abbreviation FANCM
Name Fanconi anemia, complementation group M
OMIM ID 614087
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 0 genes -
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Date created 2013-07-21 20:43:53 +02:00 (CEST)
Date last edited 2025-02-24 14:29:25 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00020028 - - affected sibling of EUFA867 ? ? - - - - - - FANCM - FANCM FANCM 2 1 Arleen D. Auerbach
00020029 - PubMed: Harutyunyan 2011 polycythemia vera, subtype of myeloproliferative neoplasm; patient developed anemia and later transformed to secondary acute myeloid leukemia (sAML) M ? Austria - - - - - FANCM transformation to secondary AML, anemic phase before transformation FANCM FANCM 2 1 Ashot Harutyunyan
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