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Diseases
Genes (711)
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FGFR2
Pfeiffer Syndrome
Acrocephalosyndactylia
TTPA
Familial Isolated Vitamin E Deficiency
FGFR1
Pfeiffer Syndrome
MEGF8
Carpenter Syndrome 1
RAB23
Carpenter Syndrome 1
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
TWIST1
Pfeiffer Syndrome
Acrocephalosyndactylia
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome
TP53
Adenoid Cystic Carcinoma
Myotonic Dystrophy
MYLK
Berdon Syndrome