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Diseases
Genes (2143)
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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
LMNA
Childhood Leukemia
Limb–girdle Muscular Dystrophy
TRNL1
Merrf Syndrome
LIPA
Acid Lipase Disease
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
ACTG2
Berdon Syndrome
IL1B
Merrf Syndrome
Ophthalmia
Renpenning's Syndrome
Childhood Leukemia
Cystinosis
MYH11
Childhood Leukemia
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
DES
Childhood Leukemia
Limb–girdle Muscular Dystrophy
SGCG
Limb–girdle Muscular Dystrophy
MYOT
Limb–girdle Muscular Dystrophy