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Diseases
Genes (1121)
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FMR1
Fragile X Syndrome
Fg Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
Disinhibition
Renpenning's Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
MED12
Fragile X Syndrome
Fg Syndrome
SLC17A5
Salla Disease
FECH
Erythropoietic Protoporphyria
PQBP1
Renpenning's Syndrome
GNAQ
Sturge–weber Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Chronic Periodontitis
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
FLNA
Fg Syndrome
Intestinal Neuronal Dysplasia
RASA1
Sturge–weber Syndrome
ASS1
Citrullinemia Type I
CD55
Protein Losing Enteropathy
PTEN
Fragile X Syndrome
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome
TP53
Fibrolamellar Hepatocellular Carcinoma
Adenoid Cystic Carcinoma
MYLK
Berdon Syndrome
APP
Fragile X Syndrome
Salla Disease
Disinhibition