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Diseases
Genes (2170)
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PKD2
Autosomal Dominant Polycystic Kidney Disease
PKD1
Autosomal Dominant Polycystic Kidney Disease
Duchenne Muscular Dystrophy
DMD
Duchenne Muscular Dystrophy
ACE
Autosomal Dominant Polycystic Kidney Disease
Lymphadenopathy
Intracerebral Hemorrhage
Severe Acute Respiratory Syndrome
Duchenne Muscular Dystrophy
Primary Ovarian Insufficiency
NR5A1
Xy Gonadal Dysgenesis
Primary Ovarian Insufficiency
WT1
Xy Gonadal Dysgenesis
Lymphadenopathy
Rubella
Primary Ovarian Insufficiency
GANAB
Autosomal Dominant Polycystic Kidney Disease
CASP8
Lymphadenopathy
Encephalitis
Intracerebral Hemorrhage
FREM1
Trigonocephaly
TNF
Dyskinesia
Autosomal Dominant Polycystic Kidney Disease
Squamous Cell Skin Cancer
Lymphadenopathy
Encephalitis
Ebola
Hellp Syndrome
Severe Acute Respiratory Syndrome
Rubella
Duchenne Muscular Dystrophy
Primary Ovarian Insufficiency
CASP3
Encephalitis
Intracerebral Hemorrhage
Severe Acute Respiratory Syndrome
Duchenne Muscular Dystrophy
Primary Ovarian Insufficiency
SRY
Xy Gonadal Dysgenesis
Duchenne Muscular Dystrophy
Primary Ovarian Insufficiency
HLA-DRB1
Eosinophilia–myalgia Syndrome
Squamous Cell Skin Cancer
Lymphadenopathy
Encephalitis
Severe Acute Respiratory Syndrome
Duchenne Muscular Dystrophy
Primary Ovarian Insufficiency
PLAT
Squamous Cell Skin Cancer
Encephalitis
Intracerebral Hemorrhage
FLT1
Intracerebral Hemorrhage
Hellp Syndrome
SPP1
Lymphadenopathy
Encephalitis
Intracerebral Hemorrhage
Duchenne Muscular Dystrophy
FAS
Squamous Cell Skin Cancer
Lymphadenopathy
Encephalitis
Hellp Syndrome
VEGFA
Dyskinesia
Autosomal Dominant Polycystic Kidney Disease
Squamous Cell Skin Cancer
Lymphadenopathy
Encephalitis
Intracerebral Hemorrhage
Ebola
Hellp Syndrome
Duchenne Muscular Dystrophy
Primary Ovarian Insufficiency
BCL2
Squamous Cell Skin Cancer
Lymphadenopathy
Encephalitis
Intracerebral Hemorrhage
Duchenne Muscular Dystrophy
Primary Ovarian Insufficiency
CCL2
Autosomal Dominant Polycystic Kidney Disease
Encephalitis
Severe Acute Respiratory Syndrome
Duchenne Muscular Dystrophy