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Diseases
Genes (430)
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TRNL1
Mitochondrial Encephalomyopathy
Merrf Syndrome
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
NIPBL
Cornelia De Lange Syndrome 3
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
RAD21
Cornelia De Lange Syndrome 3
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
ACTG2
Berdon Syndrome
HDAC8
Cornelia De Lange Syndrome 3
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
MYH11
Berdon Syndrome
TRNK
Mitochondrial Encephalomyopathy
Merrf Syndrome
MYLK
Berdon Syndrome