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Diseases
Genes (403)
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MYO5B
Microvillus Inclusion Disease
TTPA
Familial Isolated Vitamin E Deficiency
SLC12A6
Andermann Syndrome
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Singleton Merten Syndrome
ALB
Melancholia
Membranoproliferative Glomerulonephritis
Protein Losing Enteropathy
PON1
Melancholia
Membranoproliferative Glomerulonephritis
CFH
Membranoproliferative Glomerulonephritis
Salmonellosis
SLC6A4
Melancholia
STX3
Microvillus Inclusion Disease
CD55
Protein Losing Enteropathy
TSLP
Membranoproliferative Glomerulonephritis
Lumbar Disc Disease
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
POMC
Melancholia
Familial Glucocorticoid Deficiency
IL6
Fibrous Dysplasia Of Bone
Melancholia
Membranoproliferative Glomerulonephritis
Lumbar Disc Disease
Familial Isolated Vitamin E Deficiency
BDNF
Melancholia
CILP
Lumbar Disc Disease
STAR
Adrenal Crisis
Familial Glucocorticoid Deficiency