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Diseases
Genes (2382)
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TTPA
Retinitis Pigmentosa 42
Familial Isolated Vitamin E Deficiency
DMD
Duchenne Muscular Dystrophy
Meningioma
Limb–girdle Muscular Dystrophy
ASL
Argininosuccinic Aciduria
Meningioma
GJA1
Duchenne Muscular Dystrophy
Oculodentodigital Dysplasia
Meningioma
NF2
Duchenne Muscular Dystrophy
Oligodendroglioma
Meningioma
Congenital Contractural Arachnodactyly
Neurofibromatosis
EFHC1
Epilepsy, Idiopathic Generalized, Susceptibility To, 10
F12
Factor Xii Deficiency
FOXP3
Oligodendroglioma
Familial Mediterranean Fever
Ipex Syndrome
FBN2
Retinitis Pigmentosa 42
Congenital Contractural Arachnodactyly
MEFV
Familial Mediterranean Fever
PMM2
Pmm2 Deficiency
Retinitis Pigmentosa 42
PDGFB
Meningioma
Primary Familial Brain Calcification
C8orf37
Retinitis Pigmentosa 42
FMR1
Fragile X-Associated Tremor/ataxia Syndrome
Fg Syndrome
PDE6B
Retinitis Pigmentosa 42
PDE6A
Retinitis Pigmentosa 42
CRX
Pinealoblastoma
Retinitis Pigmentosa 42
AKT1
Oligodendroglioma
Meningioma
Congenital Contractural Arachnodactyly
MED12
Fg Syndrome
LMNA
Fragile X-Associated Tremor/ataxia Syndrome
Meningioma
Limb–girdle Muscular Dystrophy