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Diseases
Genes (1707)
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ASL
Argininosuccinic Aciduria
Meningioma
GJA1
Oculodentodigital Dysplasia
Meningioma
SLC6A19
Hartnup Disease
POLG
Merrf Syndrome
Balo Concentric Sclerosis
F12
Factor Xii Deficiency
BLM
Bloom Syndrome
FOXP3
Ipex Syndrome
Aortic Aneurysm, Familial Abdominal, 1
PMM2
Pmm2 Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
PDGFB
Meningioma
Primary Familial Brain Calcification
OPA3
Costeff Syndrome
SLC17A5
Salla Disease
IL1B
Merrf Syndrome
Meningioma
Bronchopulmonary Dysplasia
Aortic Aneurysm, Familial Abdominal, 1
Cystinosis
NF2
Meningioma
UMOD
Medullary Cystic Kidney Disease
MED12
Fg Syndrome
PDGFRB
Meningioma
Primary Familial Brain Calcification
Bronchopulmonary Dysplasia
SUFU
Oculodentodigital Dysplasia
Meningioma
RHBDF2
Meningioma
Howel–evans Syndrome
AKT1
Meningioma
Bronchopulmonary Dysplasia
Aortic Aneurysm, Familial Abdominal, 1