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Diseases
Genes (3081)
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KRT17
Pachyonychia Congenita
Autosomal Dominant Polycystic Kidney Disease
Epithelioma
PPARG
Thyroid Cancer, Nonmedullary, 1
Metabolic Syndrome
Autosomal Dominant Polycystic Kidney Disease
Epithelioma
BRAF
Thyroid Cancer, Nonmedullary, 1
Acinar Adenocarcinoma
Metabolic Syndrome
Epithelioma
TNF
Severe Acute Respiratory Syndrome
Thyroid Cancer, Nonmedullary, 1
Gaucher's Disease
Metabolic Syndrome
Polymyositis
Progressive Supranuclear Palsy
Hepatitis A
African Trypanosomiasis
Sarcopenia
Autosomal Dominant Polycystic Kidney Disease
Epithelioma
GBA
Gaucher's Disease
Metabolic Syndrome
Progressive Supranuclear Palsy
ACE
Severe Acute Respiratory Syndrome
Thyroid Cancer, Nonmedullary, 1
Gaucher's Disease
Metabolic Syndrome
Progressive Supranuclear Palsy
Hepatitis A
Sarcopenia
Autosomal Dominant Polycystic Kidney Disease
KRT16
Pachyonychia Congenita
Metabolic Syndrome
IL6
Severe Acute Respiratory Syndrome
Thyroid Cancer, Nonmedullary, 1
Gaucher's Disease
Metabolic Syndrome
Ischemic Colitis
Polymyositis
Progressive Supranuclear Palsy
Hepatitis A
African Trypanosomiasis
Sarcopenia
Kwashiorkor
Autosomal Dominant Polycystic Kidney Disease
Epithelioma
PKD2
Autosomal Dominant Polycystic Kidney Disease
TG
Thyroid Cancer, Nonmedullary, 1
Autoimmune Thyroid Disease, Susceptibility To, 3
Thyroid Dyshormonogenesis 3
PKD1
Metabolic Syndrome
Autosomal Dominant Polycystic Kidney Disease
NKX2-1
Thyroid Cancer, Nonmedullary, 1
Acinar Adenocarcinoma
RET
Thyroid Cancer, Nonmedullary, 1
Acinar Adenocarcinoma
Metabolic Syndrome
LEP
Thyroid Cancer, Nonmedullary, 1
Gaucher's Disease
Metabolic Syndrome
Hepatitis A
Sarcopenia
Epithelioma
CCDC6
Thyroid Cancer, Nonmedullary, 1
Metabolic Syndrome
NOS3
Thyroid Cancer, Nonmedullary, 1
Metabolic Syndrome
Autosomal Dominant Polycystic Kidney Disease
MAPT
Progressive Supranuclear Palsy
IL18
Thyroid Cancer, Nonmedullary, 1
Metabolic Syndrome
Polymyositis
Hepatitis A
Autosomal Dominant Polycystic Kidney Disease
SIRT1
Thyroid Cancer, Nonmedullary, 1
Metabolic Syndrome
Hepatitis A
Sarcopenia
KRT6A
Pachyonychia Congenita