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Diseases
Genes (1295)
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RB1
Pinealoblastoma
Retinoblastoma
Trilateral Retinoblastoma
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
ACTG2
Berdon Syndrome
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
ASS1
Retinoblastoma
Citrullinemia Type I
PDGFB
Primary Familial Brain Calcification
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
CTNS
Cystinosis
MDM4
Retinoblastoma
FUT2
Norovirus Infection
TNF
Cholera
Retinoblastoma
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Pleural Effusion
SOST
Retinoblastoma
Craniodiaphyseal Dysplasia