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Diseases
Genes (776)
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CHM
Choroideremia
TGFBR2
Uterine Rupture
Abdominal Aortic Aneurysm
Aneurysm
Loeys–dietz Syndrome
VPS33B
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
TGFBR1
Uterine Rupture
Abdominal Aortic Aneurysm
Loeys–dietz Syndrome
LIPA
Lysosomal Acid Lipase Deficiency
VIPAS39
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
SNAP29
Cerebral Dysgenesis–neuropathy–ichthyosis–keratoderma Syndrome
MYO5A
Griscelli Syndrome
NF1
Abdominal Aortic Aneurysm
Watson Syndrome
Aneurysm
RAB3GAP1
Warburg Micro Syndrome 3
GNAS
Progressive Osseous Heteroplasia
MEGF8
Carpenter Syndrome 1
PTEN
Proteus-Like Syndrome
Abdominal Aortic Aneurysm
ALS2
Juvenile Primary Lateral Sclerosis
PTPN11
Metachondromatosis
RAB23
Carpenter Syndrome 1
RAC2
Neutrophil Immunodeficiency Syndrome
NOTCH3
Abdominal Aortic Aneurysm
Cadasil