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Diseases
Genes (850)
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TTPA
Familial Isolated Vitamin E Deficiency
TMC6
Epidermodysplasia Verruciformis
PQBP1
Renpenning's Syndrome
SLC20A2
Primary Familial Brain Calcification
MED12
Fg Syndrome
PDGFRB
Primary Familial Brain Calcification
FAM20A
Enamel-Renal Syndrome
IFIH1
Dengue Fever
Singleton Merten Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
RET
Potter Sequence
TMC8
Epidermodysplasia Verruciformis
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
ITGA8
Potter Sequence
PDGFB
Primary Familial Brain Calcification
ASS1
Citrullinemia Type I
CTNS
Cystinosis
TNF
Epidermodysplasia Verruciformis
Dengue Fever
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Pleural Effusion
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CD209
Dengue Fever
GREB1L
Potter Sequence