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Diseases
Genes (1849)
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GJA1
Oculodentodigital Dysplasia
Craniosynostosis 3
Meningioma
ASL
Argininosuccinic Aciduria
Meningioma
POLG
Merrf Syndrome
Balo Concentric Sclerosis
SLC6A19
Hartnup Disease
F12
Factor Xii Deficiency
BLM
Bloom Syndrome
PMM2
Pmm2 Deficiency
FOXP3
Aortic Aneurysm, Familial Abdominal, 1
Ipex Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
PDGFB
Primary Familial Brain Calcification
Meningioma
OPA3
Costeff Syndrome
MED12
Craniosynostosis 3
Fg Syndrome
SUFU
Oculodentodigital Dysplasia
Craniosynostosis 3
Meningioma
SLC17A5
Salla Disease
IL1B
Merrf Syndrome
Meningioma
Bronchopulmonary Dysplasia
Aortic Aneurysm, Familial Abdominal, 1
Cystinosis
NF2
Meningioma
UMOD
Medullary Cystic Kidney Disease
PDGFRB
Primary Familial Brain Calcification
Meningioma
Bronchopulmonary Dysplasia
RHBDF2
Meningioma
Howel–evans Syndrome
SLC20A2
Primary Familial Brain Calcification