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Diseases
Genes (751)
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TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
ASS1
Citrullinemia Type I
PDGFB
Primary Familial Brain Calcification
CTNS
Cystinosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CNBP
Myotonic Dystrophy
FUT2
Norovirus Infection
TNF
Cholera
Myotonic Dystrophy
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Pleural Effusion
HLA-DQB1
Kleine–levin Syndrome
DDX58
Singleton Merten Syndrome
SOST
Craniodiaphyseal Dysplasia