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Diseases
Genes (606)
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ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
NIPBL
Cornelia De Lange Syndrome 3
PMM2
Pmm2 Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
RAD21
Cornelia De Lange Syndrome 3
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
HDAC8
Cornelia De Lange Syndrome 3
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
CTNS
Cystinosis
SMC3
Cornelia De Lange Syndrome 3
SMC1A
Cornelia De Lange Syndrome 3