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Diseases
Genes (844)
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MYO5B
Microvillus Inclusion Disease
FBN2
Congenital Contractural Arachnodactyly
LBR
Hydrops-Ectopic Calcification-Moth-Eaten Skeletal Dysplasia
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
GALE
Galactose Epimerase Deficiency
MC2R
Familial Glucocorticoid Deficiency
CFH
Membranoproliferative Glomerulonephritis
STX3
Microvillus Inclusion Disease
CD55
Protein Losing Enteropathy
TSLP
Membranoproliferative Glomerulonephritis
Lumbar Disc Disease
CTNS
Cystinosis
DNAJB1
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
PRKACA
Fibrolamellar Hepatocellular Carcinoma
SOST
Craniodiaphyseal Dysplasia
CILP
Lumbar Disc Disease
ALB
Membranoproliferative Glomerulonephritis
Protein Losing Enteropathy
Congenital Contractural Arachnodactyly
STAR
Adrenal Crisis
Familial Glucocorticoid Deficiency
COL9A3
Lumbar Disc Disease