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Diseases
Genes (1321)
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CSF2RA
Surfactant Metabolism Dysfunction, Pulmonary, 4
Pulmonary Alveolar Proteinosis
ITGB3
Glanzmann's Thrombasthenia
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
CSF2RB
Surfactant Metabolism Dysfunction, Pulmonary, 4
Pulmonary Alveolar Proteinosis
ITGA2B
Glanzmann's Thrombasthenia
SLC17A5
Salla Disease
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
RARA
Acute Promyelocytic Leukemia
Bronchopulmonary Dysplasia
NPM1
Acute Promyelocytic Leukemia
IFIH1
Singleton Merten Syndrome
NUMA1
Acute Promyelocytic Leukemia
PRKAR1A
Acute Promyelocytic Leukemia
Enamel-Renal Syndrome
ZBTB16
Acute Promyelocytic Leukemia
Salla Disease
PML
Acute Promyelocytic Leukemia
VEGFA
Corneal Neovascularization
Acute Promyelocytic Leukemia
Salla Disease
Subacromial Bursitis
Diverticulitis
Bronchopulmonary Dysplasia
STAT5B
Acute Promyelocytic Leukemia
IRF2BP2
Acute Promyelocytic Leukemia