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Diseases
Genes (965)
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TTPA
Familial Isolated Vitamin E Deficiency
SLC6A19
Hartnup Disease
CPT1A
Carnitine Palmitoyltransferase I Deficiency
OPA3
Costeff Syndrome
GALT
Galactose-1-Phosphate Uridylyltransferase Deficiency
PQBP1
Renpenning's Syndrome
UMOD
Medullary Cystic Kidney Disease
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
AGGF1
Klippel-Trenaunay-Weber Syndrome
CTNS
Cystinosis
Splenomegaly
TRNL1
Merrf Syndrome
ALB
Aseptic Meningitis
Membranoproliferative Glomerulonephritis
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
FLNA
Intestinal Neuronal Dysplasia
Phyllodes Tumor
CFH
Membranoproliferative Glomerulonephritis
OFD1
Orofaciodigital Syndrome 1
IL1B
Callosity
Cystinosis
Renpenning's Syndrome
Glucagonoma
Merrf Syndrome
Membranoproliferative Glomerulonephritis
ASS1
Citrullinemia Type I