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Diseases
Genes (372)
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ASL
Argininosuccinic Aciduria
MYO5B
Microvillus Inclusion Disease
PMM2
Pmm2 Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
SLC12A6
Andermann Syndrome
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PQBP1
Renpenning's Syndrome
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Singleton Merten Syndrome
PON1
Melancholia
Membranoproliferative Glomerulonephritis
ALB
Melancholia
Membranoproliferative Glomerulonephritis
CFH
Membranoproliferative Glomerulonephritis
Salmonellosis
SLC6A4
Melancholia
STX3
Microvillus Inclusion Disease
TSLP
Membranoproliferative Glomerulonephritis
Lumbar Disc Disease
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
POMC
Melancholia
Familial Glucocorticoid Deficiency
BDNF
Melancholia
IL6
Melancholia
Argininosuccinic Aciduria
Membranoproliferative Glomerulonephritis
Lumbar Disc Disease
Familial Isolated Vitamin E Deficiency