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Mediterranean Founder Mutation Database (MFMD)

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By Disease
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z [0-9]

By Gene
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Last update
21/6/2017

Disease list


L-2-hydroxyglutaric aciduria
Laing distal myopathy
Leber congenital amaurosis 1
Leber congenital amaurosis 12
Leigh syndrome
Leri-Weill dyschondrosteosis
Leukodystrophy, hypomyelinating, 2
Lipoprotein lipase deficiency
Lysosomal acid lipase deficiency

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Pasteur Institute of Morocco, Laboratory of Human Molecular Genetics © 2014 All rights reserved.

Created by Hicham Charoute.