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Diseases
Genes (932)
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FBN2
Congenital Contractural Arachnodactyly
MYO5B
Microvillus Inclusion Disease
BRAF
Langerhans Cell Histiocytosis
Congenital Contractural Arachnodactyly
PQBP1
Renpenning's Syndrome
GALE
Galactose Epimerase Deficiency
IFIH1
Hepatitis E
Singleton Merten Syndrome
CFH
Membranoproliferative Glomerulonephritis
CD55
Protein Losing Enteropathy
TSLP
Membranoproliferative Glomerulonephritis
Lumbar Disc Disease
STX3
Microvillus Inclusion Disease
CTNS
Cystinosis
DNAJB1
Congenital Contractural Arachnodactyly
Fibrolamellar Hepatocellular Carcinoma
PRKACA
Fibrolamellar Hepatocellular Carcinoma
SOST
Craniodiaphyseal Dysplasia
Langerhans Cell Histiocytosis
ALB
Hepatitis E
Membranoproliferative Glomerulonephritis
Congenital Contractural Arachnodactyly
Protein Losing Enteropathy
CILP
Lumbar Disc Disease
DDX58
Hepatitis E
Singleton Merten Syndrome
COL9A3
Lumbar Disc Disease
SART3
Disseminated Superficial Actinic Porokeratosis
GALK1
Galactose Epimerase Deficiency