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Diseases
Genes (425)
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TTPA
Familial Isolated Vitamin E Deficiency
SLC6A19
Hartnup Disease
FMR1
Renpenning's Syndrome
Fg Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
TMC6
Epidermodysplasia Verruciformis
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
TAF1
Dystonia 3, Torsion, X-Linked
GNAQ
Sturge–weber Syndrome
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
RHBDF2
Howel–evans Syndrome
IFIH1
Singleton Merten Syndrome
TMC8
Epidermodysplasia Verruciformis
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
RASA1
Sturge–weber Syndrome
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome