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Diseases
Genes (1684)
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ASL
Argininosuccinic Aciduria
Meningioma
GJA1
Oculodentodigital Dysplasia
Cholangiocarcinoma
Meningioma
BAP1
Cholangiocarcinoma
Meningioma
POLG
Merrf Syndrome
Balo Concentric Sclerosis
SLC6A19
Hartnup Disease
MYO5B
Microvillus Inclusion Disease
F12
Factor Xii Deficiency
BLM
Bloom Syndrome
PMM2
Pmm2 Deficiency
PDGFB
Primary Familial Brain Calcification
Meningioma
OPA3
Costeff Syndrome
SLC17A5
Salla Disease
TP53
Disseminated Superficial Actinic Porokeratosis
Germinoma
Bloom Syndrome
Cholangiocarcinoma
Meningioma
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PTEN
Salmonellosis
Cholangiocarcinoma
Meningioma
AKT1
Cholangiocarcinoma
Meningioma
NF2
Meningioma
SUFU
Oculodentodigital Dysplasia
Meningioma
PDGFRB
Primary Familial Brain Calcification
Cholangiocarcinoma
Meningioma
SLC20A2
Primary Familial Brain Calcification