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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


Hematuria, benign familial
Hemochromatosis
Hemolytic anemia due to G6PD deficiency (Glucose-6-phosphate dehydrogenase deficiency)
Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy
Hemophagocytic lymphohistiocytosis, familial, 2
Hemophilia A
Hemophilia B
Hirschsprung disease, susceptibility to, 1
Huntington disease
Hydatidiform mole
Hypercholesterolemia, familial
Hyperekplexia, hereditary 1, autosomal dominant or recessive
Hyperinsulinemic hypoglycemia, familial, 1
Hyperoxaluria, primary, type 1
Hyperphenylalaninemia, BH4-deficient, C
Hyperuricemic nephropathy, familial juvenile 1
Hypomagnesemia 3, renal
Hypomagnesemia 5, renal, with ocular involvement
Hypophosphatasia, childhood
Hypotrichosis 4

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

Created by Hicham Charoute.