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Diseases
Genes (1914)
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ACE
Heart Arrhythmia
Glycogen Storage Disease Type V
Chronic Periodontitis
Bronchopulmonary Dysplasia
Acute Coronary Syndrome
Early-Onset Autosomal Dominant Alzheimer Disease
TTPA
Heart Arrhythmia
Familial Isolated Vitamin E Deficiency
PYGM
Gastrinoma
Glycogen Storage Disease Type V
TNF
Heart Arrhythmia
Cystic Echinococcosis
Salla Disease
Machado–joseph Disease
Chronic Periodontitis
Bronchopulmonary Dysplasia
Subacromial Bursitis
Familial Isolated Vitamin E Deficiency
Acute Coronary Syndrome
Early-Onset Autosomal Dominant Alzheimer Disease
Autoimmune Hemolytic Anemia
GNAQ
Heart Arrhythmia
Sturge–weber Syndrome
SLC12A6
Andermann Syndrome
IL1B
Heart Arrhythmia
Glucagonoma
Chronic Periodontitis
Bronchopulmonary Dysplasia
Subacromial Bursitis
Acute Coronary Syndrome
Early-Onset Autosomal Dominant Alzheimer Disease
MED12
Fg Syndrome
MEN1
Gastrinoma
Glucagonoma
SOD2
Heart Arrhythmia
Machado–joseph Disease
Chronic Periodontitis
Bronchopulmonary Dysplasia
Acute Coronary Syndrome
Early-Onset Autosomal Dominant Alzheimer Disease
SLC17A5
Salla Disease
UMOD
Medullary Cystic Kidney Disease
Acute Coronary Syndrome
SLC2A10
Arterial Tortuosity Syndrome
FECH
Erythropoietic Protoporphyria
UBA1
X-Linked Spinal Muscular Atrophy Type 2
IL6
Fibrous Dysplasia Of Bone
Heart Arrhythmia
Machado–joseph Disease
Chronic Periodontitis
Bronchopulmonary Dysplasia
Subacromial Bursitis
Familial Isolated Vitamin E Deficiency
Acute Coronary Syndrome
Early-Onset Autosomal Dominant Alzheimer Disease
Autoimmune Hemolytic Anemia
GJA1
Heart Arrhythmia
MMP9
Chronic Periodontitis
Bronchopulmonary Dysplasia
Acute Coronary Syndrome
ATXN3
Machado–joseph Disease
FLNA
Fg Syndrome
Intestinal Neuronal Dysplasia
Bronchopulmonary Dysplasia