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Diseases
Genes (2380)
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PKD2
Autosomal Dominant Polycystic Kidney Disease
DMD
Duchenne Muscular Dystrophy
PKD1
Autosomal Dominant Polycystic Kidney Disease
Duchenne Muscular Dystrophy
ACE
Autosomal Dominant Polycystic Kidney Disease
Lymphadenopathy
Intracerebral Hemorrhage
Severe Acute Respiratory Syndrome
Duchenne Muscular Dystrophy
Dermatitis
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
HLA-DQA1
Eosinophilia–myalgia Syndrome
Squamous Cell Skin Cancer
Duchenne Muscular Dystrophy
Dermatitis
TNF
Dyskinesia
Autosomal Dominant Polycystic Kidney Disease
Squamous Cell Skin Cancer
Lymphadenopathy
Encephalitis
Ebola
Severe Acute Respiratory Syndrome
Hellp Syndrome
Duchenne Muscular Dystrophy
Dermatitis
Rubella
Primary Ovarian Insufficiency
CASP8
Lymphadenopathy
Intracerebral Hemorrhage
Encephalitis
Dermatitis
FREM1
Trigonocephaly
CASP3
Intracerebral Hemorrhage
Encephalitis
Severe Acute Respiratory Syndrome
Duchenne Muscular Dystrophy
Primary Ovarian Insufficiency
HLA-B
Lymphadenopathy
Encephalitis
Ebola
Severe Acute Respiratory Syndrome
Duchenne Muscular Dystrophy
Dermatitis
SRY
Xy Gonadal Dysgenesis
Duchenne Muscular Dystrophy
Primary Ovarian Insufficiency
PLAT
Squamous Cell Skin Cancer
Intracerebral Hemorrhage
Encephalitis
Dermatitis
HLA-DRB1
Eosinophilia–myalgia Syndrome
Squamous Cell Skin Cancer
Lymphadenopathy
Encephalitis
Severe Acute Respiratory Syndrome
Duchenne Muscular Dystrophy
Primary Ovarian Insufficiency
FLT1
Intracerebral Hemorrhage
Hellp Syndrome
SPP1
Lymphadenopathy
Intracerebral Hemorrhage
Encephalitis
Duchenne Muscular Dystrophy
CCL2
Autosomal Dominant Polycystic Kidney Disease
Encephalitis
Severe Acute Respiratory Syndrome
Duchenne Muscular Dystrophy
Dermatitis
RELA
Squamous Cell Skin Cancer
Intracerebral Hemorrhage
Encephalitis
Duchenne Muscular Dystrophy
Dermatitis