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Diseases
Genes (419)
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MYO5B
Microvillus Inclusion Disease
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
CD55
Protein Losing Enteropathy
STX3
Microvillus Inclusion Disease
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
BDNF
Melancholia
PTGS2
Fibrous Dysplasia Of Bone
Melancholia
Epidermoid Cysts
Salmonellosis
CILP
Lumbar Disc Disease
STAR
Adrenal Crisis
Familial Glucocorticoid Deficiency