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Diseases
Genes (2340)
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ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
TNF
Ophthalmia
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Tetraplegia
Childhood Leukemia
Myotonic Dystrophy
Asystole
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
LIPA
Acid Lipase Disease
Asystole
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
TRNL1
Merrf Syndrome
IL1B
Merrf Syndrome
Ophthalmia
Renpenning's Syndrome
Childhood Leukemia
Cystinosis
Asystole
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
ACTG2
Berdon Syndrome
MYH11
Childhood Leukemia
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
IFNG
Ophthalmia
Vascular Tumor
Childhood Leukemia
Cystinosis
Asystole
DMPK
Myotonic Dystrophy
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I