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Diseases
Genes (2330)
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GJA1
Oculodentodigital Dysplasia
Meningioma
POLG
Merrf Syndrome
Balo Concentric Sclerosis
SLC6A19
Hartnup Disease
EFHC1
Epilepsy, Idiopathic Generalized, Susceptibility To, 10
NF2
Neurofibromatosis
Meningioma
Retinoblastoma
BLM
Bloom Syndrome
F12
Factor Xii Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
PDGFB
Primary Familial Brain Calcification
Meningioma
OPA3
Costeff Syndrome
IL1B
Merrf Syndrome
Meningioma
Retinoblastoma
Bronchopulmonary Dysplasia
Aortic Aneurysm, Familial Abdominal, 1
AKT1
Meningioma
Retinoblastoma
Bronchopulmonary Dysplasia
Aortic Aneurysm, Familial Abdominal, 1
SLC17A5
Salla Disease
RB1
Pinealoblastoma
Meningioma
Retinoblastoma
FECH
Erythropoietic Protoporphyria
UMOD
Medullary Cystic Kidney Disease
MMP9
Meningioma
Retinoblastoma
Bronchopulmonary Dysplasia
Aortic Aneurysm, Familial Abdominal, 1
PDGFRB
Primary Familial Brain Calcification
Meningioma
Bronchopulmonary Dysplasia
SUFU
Oculodentodigital Dysplasia
Meningioma
RHBDF2
Meningioma
Howel–evans Syndrome