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Diseases
Genes (619)
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TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
SLC20A2
Primary Familial Brain Calcification
FAM20A
Enamel-Renal Syndrome
PDGFRB
Primary Familial Brain Calcification
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
PDGFB
Callosity
Primary Familial Brain Calcification
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
SLC4A4
Proximal Renal Tubular Acidosis
CTNS
Cystinosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
LEMD3
Melorheostosis
SOST
Callosity
Craniodiaphyseal Dysplasia
ITGB3
Coronary Thrombosis