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Diseases
Genes (197)
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PRNP
Variant Creutzfeldt–jakob Disease
Kuru, Susceptibility To
Akinetic Mutism
LIPA
Lysosomal Acid Lipase Deficiency
TBX5
Holt–oram Syndrome
TGFBR2
Uterine Rupture
Aneurysm
Loeys–dietz Syndrome
Dural Arteriovenous Fistula
TGFBR1
Uterine Rupture
Loeys–dietz Syndrome
SLC4A1
Southeast Asian Ovalocytosis
IFIH1
Singleton Merten Syndrome
TGFB2
Loeys–dietz Syndrome
Holt–oram Syndrome
SRD5A2
5α-Reductase Deficiency
FAM155A
Diverticulitis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
SMAD3
Aneurysm
Loeys–dietz Syndrome
SALL4
Holt–oram Syndrome
DDX58
Singleton Merten Syndrome
MMP1
Aneurysm
Diverticulitis
ALDH1A1
Variant Creutzfeldt–jakob Disease
H4C4
Variant Creutzfeldt–jakob Disease
SNORA16B
Variant Creutzfeldt–jakob Disease
KRT73
Variant Creutzfeldt–jakob Disease
MSL3P1
Variant Creutzfeldt–jakob Disease