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Diseases
Genes (716)
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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
MMUT
Methylmalonyl-Coa Mutase Deficiency
MED12
Fragile X Syndrome
Fg Syndrome
SLC17A5
Salla Disease
PQBP1
Renpenning's Syndrome
GNAQ
Sturge–weber Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
FLNA
Fg Syndrome
Intestinal Neuronal Dysplasia
RASA1
Sturge–weber Syndrome
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
APP
Fragile X Syndrome
Salla Disease
Disinhibition
MYLK
Berdon Syndrome
CTNS
Cystinosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
Hemangioendothelioma
PRKACA
Fibrolamellar Hepatocellular Carcinoma