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Diseases
Genes (1340)
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ASL
Argininosuccinic Aciduria
Liver Failure
PMM2
Pmm2 Deficiency
FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
TNF
Acute Liver Failure
Liver Failure
Congenital Contractural Arachnodactyly
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Langerhans Cell Histiocytosis
Dysentery
Aneurysm
ALB
Acute Liver Failure
Liver Failure
Membranoproliferative Glomerulonephritis
Congenital Contractural Arachnodactyly
Disinhibition
BRAF
Congenital Contractural Arachnodactyly
Langerhans Cell Histiocytosis
PQBP1
Renpenning's Syndrome
ASS1
Argininosuccinic Aciduria
Liver Failure
Congenital Contractural Arachnodactyly
Citrullinemia Type I
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
GALE
Galactose Epimerase Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ATP7B
Acute Liver Failure
Liver Failure
ACTG2
Congenital Contractural Arachnodactyly
Berdon Syndrome
CFH
Membranoproliferative Glomerulonephritis
MYH11
Aneurysm
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
MYLK
Aneurysm
Berdon Syndrome