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Diseases
Genes (814)
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TTPA
Familial Isolated Vitamin E Deficiency
ATP7B
Wilson's Disease
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
TNF
Cholera
Myotonic Dystrophy
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Wilson's Disease
Pleural Effusion
DMPK
Myotonic Dystrophy
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
ASS1
Citrullinemia Type I
ANXA5
Cholera
Wilson's Disease
PDGFB
Primary Familial Brain Calcification
CTNS
Cystinosis
IL6
Cholera
Myotonic Dystrophy
Familial Isolated Vitamin E Deficiency
Wilson's Disease
Pleural Effusion
IL10
Wilson's Disease
Pleural Effusion
Cystinosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
Wilson's Disease
CNBP
Myotonic Dystrophy