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Diseases
Genes (705)
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TRNL1
Mitochondrial Encephalomyopathy
Merrf Syndrome
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
SMC1A
Cornelia De Lange Syndrome 3
Adenoid Cystic Carcinoma
IFIH1
Singleton Merten Syndrome
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
HDAC8
Fibrous Dysplasia Of Bone
Cornelia De Lange Syndrome 3
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Microscopic Colitis
Adenoid Cystic Carcinoma
TRNK
Mitochondrial Encephalomyopathy
Merrf Syndrome
TP53
Adenoid Cystic Carcinoma
CTNS
Cystinosis