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Diseases
Genes (940)
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TTPA
Familial Isolated Vitamin E Deficiency
FMR1
Fragile X-Associated Tremor/ataxia Syndrome
Renpenning's Syndrome
Fg Syndrome
PQBP1
Renpenning's Syndrome
TMC6
Epidermodysplasia Verruciformis
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
Chronic Periodontitis
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
TMC8
Epidermodysplasia Verruciformis
TP53
Epidermodysplasia Verruciformis
Adenoid Cystic Carcinoma
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Epidermodysplasia Verruciformis
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
CTNS
Cystinosis
NOTCH1
Adenoid Cystic Carcinoma
Melorheostosis
SHH
Cyclopia