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Diseases
Genes (1873)
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SLC4A1
Cryohydrocytosis
Dehydrated Hereditary Stomatocytosis
Spherocytosis, Type 4
TNF
Pleural Effusion
Cryohydrocytosis
Inflammation
Syndromic Recessive X-Linked Ichthyosis
Dactylitis
Keratoconus
Otitis
Angiogenesis
VEGFA
Pleural Effusion
Cryohydrocytosis
Corneal Neovascularization
Inflammation
Syndromic Recessive X-Linked Ichthyosis
Angiogenesis
Coats Disease
Primitive Portal Vein Thrombosis
FGF2
Corneal Neovascularization
Inflammation
Angiogenesis
STS
Inflammation
Syndromic Recessive X-Linked Ichthyosis
IL6
Pleural Effusion
Cryohydrocytosis
Corneal Neovascularization
Inflammation
Syndromic Recessive X-Linked Ichthyosis
Keratoconus
Otitis
Angiogenesis
Coats Disease
Primitive Portal Vein Thrombosis
IL10
Pleural Effusion
Cryohydrocytosis
Inflammation
Otitis
Angiogenesis
PDGFRB
Corneal Neovascularization
Primary Familial Brain Calcification
Inflammation
Angiogenesis
TRPV4
Autosomal Dominant Brachyolmia
Angiogenesis
CRP
Pleural Effusion
Cryohydrocytosis
Colchicine Resistance
Inflammation
Syndromic Recessive X-Linked Ichthyosis
Primitive Portal Vein Thrombosis
GALE
Galactose Epimerase Deficiency
SLC20A2
Primary Familial Brain Calcification
ABCB6
Pseudohyperkalemia, Familial, 2, Due To Red Cell Leak
Angiogenesis
IL1B
Pleural Effusion
Corneal Neovascularization
Inflammation
Syndromic Recessive X-Linked Ichthyosis
Keratoconus
Otitis
Angiogenesis
Coats Disease
RHAG
Overhydrated Hereditary Stomatocytosis
ABCB1
Colchicine Resistance
Inflammation
Syndromic Recessive X-Linked Ichthyosis
XPNPEP2
Renin-Angiotensin-Aldosterone System-Blocker-Induced Angioedema
Angioedema
MIF
Pleural Effusion
Inflammation
CCL2
Pleural Effusion
Corneal Neovascularization
Inflammation
Syndromic Recessive X-Linked Ichthyosis
Angiogenesis
Coats Disease
PTGS2
Inflammation
Angiogenesis