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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


Achalasia-addisonianism-alacrimia syndrome
Achromatopsia-4
Acrodermatitis enteropathica
Adenomas, multiple colorectal
Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
Adrenoleukodystrophy
Afibrinogenemia, congenital
Alkaptonuria
Alport syndrome, autosomal recessive
Alzheimer disease 1, familial
Alzheimer disease, type 3
Amyloidosis, hereditary, transthyretin-related
Amyotrophic lateral sclerosis 1
Amyotrophic lateral sclerosis and/or frontotemporal dementia
Angioedema, hereditary, type III
Arthropathy, progressive pseudorheumatoid, of childhood
Ataxia with isolated vitamin E deficiency
Ataxia-telangiectasia
Autoimmune polyendocrinopathy syndrome , type I

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

Created by Hicham Charoute.