Disease #03543 (FANCL (Fanconi anemia, complementation group L (FANCL)), OMIM:614083)

Official abbreviation FANCL
Name Fanconi anemia, complementation group L (FANCL)
OMIM ID 614083
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene FANCL
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00020031 - - - ? ? - - - - - - FANCL - FANCL FANCL 2 1 Arleen D. Auerbach
00020032 - - - M ? - - - - - - FANCL - FANCL FANCL 2 1 Arleen D. Auerbach
00020033 - PubMed: Chandrasekharappa 2013 - ? ? - - - - - - FANCL - FANCL FANCL 2 1 Arleen D. Auerbach
00020034 - PubMed: Chandrasekharappa 2013 - ? ? - - - - - - FANCL - FANCL FANCL 2 1 Arleen D. Auerbach
00020035 - PubMed: Chandrasekharappa 2013 - ? ? - - - - - - FANCL - FANCL FANCL 2 1 Arleen D. Auerbach
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