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Diseases
Genes (882)
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MED12
Phyllodes Tumor
Fg Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
SLC6A19
Hartnup Disease
CPT1A
Carnitine Palmitoyltransferase I Deficiency
FLNA
Intestinal Neuronal Dysplasia
Phyllodes Tumor
Fg Syndrome
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
CTNS
Cystinosis
Splenomegaly
TRNL1
Merrf Syndrome
ALB
Aseptic Meningitis
Membranoproliferative Glomerulonephritis
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
CFH
Membranoproliferative Glomerulonephritis
OFD1
Orofaciodigital Syndrome 1
ASS1
Citrullinemia Type I
IL1B
Cystinosis
Renpenning's Syndrome
Glucagonoma
Merrf Syndrome
Membranoproliferative Glomerulonephritis