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Diseases
Genes (488)
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ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
SLC6A19
Phenylketonuria (Pku)
Hartnup Disease
SCN5A
Cardiac Conduction Defect
Enamel-Renal Syndrome
PMM2
Pmm2 Deficiency
PAH
Phenylketonuria (Pku)
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
FLVCR2
Fowler's Syndrome
IFIH1
Singleton Merten Syndrome
Common Cold
ASS1
Argininosuccinic Aciduria
Phenylketonuria (Pku)
Citrullinemia Type I
RB1
Pinealoblastoma
Trilateral Retinoblastoma
IL6
Argininosuccinic Aciduria
Toxoplasmosis
Aseptic Meningitis
Irritant Contact Dermatitis
Familial Isolated Vitamin E Deficiency
Common Cold
STAT6
Hemangiopericytoma
NAB2
Hemangiopericytoma
QDPR
Phenylketonuria (Pku)
DDX58
Singleton Merten Syndrome
TRPM4
Cardiac Conduction Defect
ALB
Phenylketonuria (Pku)
Aseptic Meningitis
SCN1B
Cardiac Conduction Defect
Enamel-Renal Syndrome