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Diseases
Genes (624)
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TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
SLC20A2
Cyclopia
Primary Familial Brain Calcification
FAM20A
Enamel-Renal Syndrome
PDGFRB
Primary Familial Brain Calcification
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
AGGF1
Klippel-Trenaunay-Weber Syndrome
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
ASS1
Citrullinemia Type I
PDGFB
Primary Familial Brain Calcification
CTNS
Cystinosis
SHH
Cyclopia
RB1
Pinealoblastoma
Trilateral Retinoblastoma
FUT2
Norovirus Infection
SOST
Klippel-Trenaunay-Weber Syndrome
Craniodiaphyseal Dysplasia
DDX58
Singleton Merten Syndrome
TNF
Cholera
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Pleural Effusion
CASK
Fg Syndrome