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Diseases
Genes (1780)
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TTPA
Familial Isolated Vitamin E Deficiency
TRIP11
Achondrogenesis
Achondrogenesis
SOD1
Callosity
Amyotrophic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
CYP19A1
Myoma
Amyotrophic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
Aromatase Deficiency
OPTN
Myopia 23, Autosomal Recessive
Amyotrophic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
C9orf72
Amyotrophic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
PQBP1
Renpenning's Syndrome
IFIH1
Myopia 23, Autosomal Recessive
Singleton Merten Syndrome
PMPCA
Spinocerebellar Ataxia, Autosomal Recessive 2
SQSTM1
Callosity
Amyotrophic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
PON1
Amyotrophic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
ATXN2
Amyotrophic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
FUS
Amyotrophic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
TARDBP
Amyotrophic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
TAF15
Amyotrophic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
MATR3
Amyotrophic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
TBK1
Amyotrophic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
UNC13A
Amyotrophic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
CHMP2B
Amyotrophic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
NEK1
Amyotrophic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia