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Diseases
Genes (2369)
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TNF
Lyme Disease
Toxoplasmosis
Actinic Keratosis
Encephalitis
Chronic Obstructive Pulmonary Disease
Sun Allergy
Hypercalcaemia
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Sjogren's Syndrome
Hypothermia
CYP27B1
Rickets
Hypercalcaemia
COL6A1
Bethlem Myopathy
Chronic Obstructive Pulmonary Disease
ASL
Argininosuccinic Aciduria
PTH
Chronic Obstructive Pulmonary Disease
Rickets
Hypercalcaemia
IL6
Lyme Disease
Argininosuccinic Aciduria
Toxoplasmosis
Encephalitis
Chronic Obstructive Pulmonary Disease
Hypercalcaemia
Familial Isolated Vitamin E Deficiency
Sjogren's Syndrome
Hypothermia
RYR2
Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
TTPA
Familial Isolated Vitamin E Deficiency
MMP1
Lyme Disease
Actinic Keratosis
Chronic Obstructive Pulmonary Disease
PMM2
Pmm2 Deficiency
HMOX1
Encephalitis
Chronic Obstructive Pulmonary Disease
Sjogren's Syndrome
VDR
Actinic Keratosis
Chronic Obstructive Pulmonary Disease
Rickets
Hypercalcaemia
Sjogren's Syndrome
TGFB1
Lyme Disease
Toxoplasmosis
Chronic Obstructive Pulmonary Disease
Sjogren's Syndrome
COL6A3
Bethlem Myopathy
COL6A2
Bethlem Myopathy
Chronic Obstructive Pulmonary Disease
PQBP1
Renpenning's Syndrome
STAT4
Encephalitis
Chronic Obstructive Pulmonary Disease
Sjogren's Syndrome
IL12A
Lyme Disease
Encephalitis
Chronic Obstructive Pulmonary Disease
Sjogren's Syndrome
Hypothermia
TRDN
Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
CALM1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 2