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Diseases
Genes (1220)
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NPM1
Acute Promyelocytic Leukemia
Dyskeratosis Congenita
AFG3L2
Spinocerebellar Ataxia Type 28
DKC1
Dyskeratosis Congenita
TINF2
Dyskeratosis Congenita
FOXP2
Speech-Language Disorder 1
CYP19A1
Aromatase Deficiency
SLC20A2
Cyclopia
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
Acute Promyelocytic Leukemia
TERC
Hydatidiform Mole, Recurrent, 1
Acute Promyelocytic Leukemia
Dyskeratosis Congenita
RARA
Acute Promyelocytic Leukemia
SON
Zttk Syndrome
RTEL1
Dyskeratosis Congenita
PARN
Dyskeratosis Congenita
WRAP53
Dyskeratosis Congenita
TERT
Hydatidiform Mole, Recurrent, 1
Acute Promyelocytic Leukemia
Dyskeratosis Congenita
CTC1
Dyskeratosis Congenita
NUMA1
Acute Promyelocytic Leukemia
RYR2
Tachycardia
Ventricular Tachycardia, Familial
ZBTB16
Hydatidiform Mole, Recurrent, 1
Acute Promyelocytic Leukemia
TGM1
Bathing Suit Ichthyosis
Acute Promyelocytic Leukemia