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Diseases
Genes (499)
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SLC6A19
Phenylketonuria (Pku)
Hartnup Disease
TTPA
Familial Isolated Vitamin E Deficiency
SCN5A
Cardiac Conduction Defect
PAH
Phenylketonuria (Pku)
PQBP1
Renpenning's Syndrome
FLVCR2
Fowler's Syndrome
IFIH1
Singleton Merten Syndrome
CD55
Protein Losing Enteropathy
SYCP3
Spermatogenesis Arrest
IL6
Fibrous Dysplasia Of Bone
Toxoplasmosis
Aseptic Meningitis
Irritant Contact Dermatitis
Familial Isolated Vitamin E Deficiency
RB1
Pinealoblastoma
Trilateral Retinoblastoma
STAT6
Hemangiopericytoma
NAB2
Hemangiopericytoma
QDPR
Phenylketonuria (Pku)
DDX58
Singleton Merten Syndrome
TRPM4
Cardiac Conduction Defect
ALB
Phenylketonuria (Pku)
Protein Losing Enteropathy
Aseptic Meningitis
FH
Fumarase Deficiency
C2
Irritant Contact Dermatitis
CBR1
Irritant Contact Dermatitis