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Diseases
Genes (520)
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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
ASS1
Citrullinemia Type I
PDGFB
Primary Familial Brain Calcification
ALAD
Lead Poisoning
CTNS
Cystinosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
HFE
Lead Poisoning
Pleural Effusion
DDX58
Singleton Merten Syndrome
SOST
Craniodiaphyseal Dysplasia
CASK
Fg Syndrome
ADAM17
Blister
VDR
Lead Poisoning