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Diseases
Genes (886)
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PQBP1
Microlissencephaly
Renpenning's Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
HMBS
Acute Intermittent Porphyria
FAM20A
Enamel-Renal Syndrome
SGPL1
Nephrotic Syndrome, Type 14
IFIH1
Singleton Merten Syndrome
DMPK
Myotonic Dystrophy
ASS1
Citrullinemia Type I
CD55
Protein Losing Enteropathy
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
TP53
Myotonic Dystrophy
Adenoid Cystic Carcinoma
Acute Intermittent Porphyria
NOTCH1
Ameloblastic Carcinoma
Adenoid Cystic Carcinoma
VEGFA
Corneal Neovascularization
Adenoid Cystic Carcinoma
PIK3CA
Adenoid Cystic Carcinoma
RB1
Pinealoblastoma
Trilateral Retinoblastoma
KRT5
Onychogryphosis
Adenoid Cystic Carcinoma
CNBP
Myotonic Dystrophy
KATNB1
Microlissencephaly
JMJD1C
Corneal Neovascularization
Adenoid Cystic Carcinoma
MYBL1
Adenoid Cystic Carcinoma