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Diseases
Genes (305)
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PRNP
Kuru
Variant Creutzfeldt–jakob Disease
AFG3L2
Spinocerebellar Ataxia Type 28
SLC4A1
Southeast Asian Ovalocytosis
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
TGM1
Bathing Suit Ichthyosis
PDGFB
Primary Familial Brain Calcification
CREB1
Angiomatoid Fibrous Histiocytoma
ALOX12B
Bathing Suit Ichthyosis
ABCA12
Bathing Suit Ichthyosis
ALOXE3
Bathing Suit Ichthyosis
DIAPH3
Auditory Neuropathy
RYR2
Ventricular Tachycardia, Familial
SOST
Craniodiaphyseal Dysplasia
TNF
Listeriosis
CALM1
Ventricular Tachycardia, Familial
CASQ2
Ventricular Tachycardia, Familial
GNAI2
Ventricular Tachycardia, Familial
TECRL
Ventricular Tachycardia, Familial
HLA-DQB1
Variant Creutzfeldt–jakob Disease
Guillain-Barré Syndrome