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Diseases
Genes (428)
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PEX1
Peroxisome Biogenesis Disorder 10a (Zellweger)
GATA2
Immunodeficiency 21
GALK1
Galactokinase Deficiency
TBX19
Acth Deficiency, Isolated
FOXP2
Foxp2-Related Speech And Language Disorder
FOXG1
Foxg1 Syndrome
IL1B
Ophthalmia
Merrf Syndrome
Membranoproliferative Glomerulonephritis
Foxp2-Related Speech And Language Disorder
FOXE3
Aortic Aneurysm, Familial Thoracic 11, Susceptibility To
LIPA
Acid Lipase Disease
COX4I2
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis
TRNL1
Merrf Syndrome
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
CFH
Membranoproliferative Glomerulonephritis
SMARCAD1
Huriez Syndrome
PEX3
Peroxisome Biogenesis Disorder 10a (Zellweger)
PEX6
Peroxisome Biogenesis Disorder 10a (Zellweger)
FOXF1
Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins
PEX16
Peroxisome Biogenesis Disorder 10a (Zellweger)
PEX2
Peroxisome Biogenesis Disorder 10a (Zellweger)