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Diseases
Genes (706)
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TTPA
Familial Isolated Vitamin E Deficiency
BEST1
Vitelliform Macular Dystrophy
BMPR1A
Juvenile Polyposis Syndrome
SMAD4
Juvenile Polyposis Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
SLC20A2
Primary Familial Brain Calcification
UBE3B
Kaufman Oculocerebrofacial Syndrome
PDGFRB
Primary Familial Brain Calcification
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
ENG
Juvenile Polyposis Syndrome
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
Juvenile Polyposis Syndrome
PDGFB
Primary Familial Brain Calcification
MYLK
Berdon Syndrome
CTNS
Cystinosis