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Diseases
Genes (660)
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FMR1
Fg Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
Fragile X Syndrome
Disinhibition
Renpenning's Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
MMUT
Methylmalonyl-Coa Mutase Deficiency
MED12
Fg Syndrome
Fragile X Syndrome
SLC17A5
Salla Disease
PQBP1
Renpenning's Syndrome
GNAQ
Sturge–weber Syndrome
FAM20A
Enamel-Renal Syndrome
TMEM67
Coach Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
RPGRIP1L
Coach Syndrome
CC2D2A
Coach Syndrome
IFIH1
Singleton Merten Syndrome
AGGF1
Klippel–trénaunay Syndrome
ACTG2
Berdon Syndrome
FLNA
Fg Syndrome
Intestinal Neuronal Dysplasia
RASA1
Klippel–trénaunay Syndrome
Sturge–weber Syndrome
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome