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Diseases
Genes (2720)
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TP53
Disseminated Superficial Actinic Porokeratosis
Osteosarcoma
Acute Erythroid Leukemia
ASL
Argininosuccinic Aciduria
MYO5B
Microvillus Inclusion Disease
PMM2
Pmm2 Deficiency
SCN1A
Dravet Syndrome
MED12
Fg Syndrome
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
CHEK2
Osteosarcoma
RB1
Osteosarcoma
Pinealoblastoma
KCNQ1
Osteosarcoma
Myotonic Dystrophy 1
Short Qt Syndrome 2
ALB
Osteosarcoma
Myotonic Dystrophy 1
Aseptic Meningitis
Membranoproliferative Glomerulonephritis
Perforated Ulcer
DMPK
Myotonic Dystrophy 1
GALE
Galactose Epimerase Deficiency
MC2R
Familial Glucocorticoid Deficiency
AGGF1
Klippel–trénaunay Syndrome
CFH
Membranoproliferative Glomerulonephritis
SCN9A
Dravet Syndrome
STX3
Microvillus Inclusion Disease
STXBP1
Dravet Syndrome
RECQL4
Osteosarcoma