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Diseases
Genes (2130)
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ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Hepatitis E
Singleton Merten Syndrome
TRNL1
Merrf Syndrome
LIPA
Acid Lipase Disease
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
IL1B
Merrf Syndrome
Ophthalmia
Renpenning's Syndrome
Childhood Leukemia
Cystinosis
DMPK
Myotonic Dystrophy
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
BRCA1
Primary Peritoneal Carcinoma
Childhood Leukemia
CTNS
Cystinosis
TRNK
Merrf Syndrome
ND5
Merrf Syndrome