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Diseases
Genes (1559)
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FLCN
Pneumothorax
Primary Spontaneous Pneumothorax
AIRE
Autoimmune Polyendocrine Syndrome Type 1
Omenn Syndrome
Liver Disease
ASL
Argininosuccinic Aciduria
RAG2
Omenn Syndrome
PMM2
Pmm2 Deficiency
Liver Disease
RAG1
Omenn Syndrome
DCLRE1C
Omenn Syndrome
Liver Disease
GALE
Galactose Epimerase Deficiency
IL1B
Bronchopulmonary Dysplasia
Membranoproliferative Glomerulonephritis
Cystinosis
Liver Disease
TXN
Bronchopulmonary Dysplasia
Liver Disease
CFH
Membranoproliferative Glomerulonephritis
Liver Disease
JAK3
Omenn Syndrome
Intestinal Obstruction
CD3D
Omenn Syndrome
Liver Disease
FOXF1
Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins
Bronchopulmonary Dysplasia
SFTPB
Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins
Infant Respiratory Distress Syndrome
Bronchopulmonary Dysplasia
CCL2
Bronchopulmonary Dysplasia
Membranoproliferative Glomerulonephritis
Cystinosis
Liver Disease
IL7R
Omenn Syndrome
Liver Disease
SFTPC
Infant Respiratory Distress Syndrome
Bronchopulmonary Dysplasia
IL2RG
Omenn Syndrome
ADA
Omenn Syndrome
Bronchopulmonary Dysplasia