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Diseases
Genes (777)
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TTPA
Familial Isolated Vitamin E Deficiency
NIPBL
Cornelia De Lange Syndrome 3
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
RAD21
Cornelia De Lange Syndrome 3
SMC1A
Cornelia De Lange Syndrome 3
Adenoid Cystic Carcinoma
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
HDAC8
Fibrous Dysplasia Of Bone
Cornelia De Lange Syndrome 3
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
ASS1
Citrullinemia Type I
CD55
Protein Losing Enteropathy
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
TP53
Adenoid Cystic Carcinoma
Myotonic Dystrophy
Esthesioneuroblastoma
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
CTNS
Cystinosis