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Diseases
Genes (1372)
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DMD
Duchenne Muscular Dystrophy
Myotonic Dystrophy
Becker Muscular Dystrophy
Mental Retardation, X-Linked 50
Haemophilia A
FMR1
Fragile X-Associated Tremor/ataxia Syndrome
Fg Syndrome
Mental Retardation, X-Linked 50
Fragile X Syndrome
Renpenning's Syndrome
MED12
Fg Syndrome
Alpha-Thalassemia Mental Retardation Syndrome
Phyllodes Tumor
Mental Retardation, X-Linked 50
Fragile X Syndrome
MID1
Opitz G/bbb Syndrome
X-Linked Opitz G/bbb Syndrome
ATRX
Alpha-Thalassemia Mental Retardation Syndrome
F8
Duchenne Muscular Dystrophy
L1 Syndrome
Haemophilia A
TBX5
Holt–oram Syndrome
L1CAM
L1 Syndrome
CCL2
Duchenne Muscular Dystrophy
Becker Muscular Dystrophy
Valvular Heart Disease
IRF6
Van Der Woude Syndrome
Fragile X Syndrome
PABPN1
Oculopharyngeal Muscular Dystrophy
OPA3
Costeff Syndrome
PMM2
Pmm2 Deficiency
ADGRG1
Bilateral Frontoparietal Polymicrogyria
UMOD
Medullary Cystic Kidney Disease
Van Der Woude Syndrome
TGFB1
Duchenne Muscular Dystrophy
Becker Muscular Dystrophy
Salla Disease
Valvular Heart Disease
Haemophilia A
ABCC9
Cantú Syndrome
MTM1
Myotonic Dystrophy
X-Linked Centronuclear Myopathy
SLC17A5
Salla Disease
PQBP1
Renpenning's Syndrome