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Diseases
Genes (2289)
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HMBS
Acute Intermittent Porphyria
HTT
Huntington's Disease
NDN
Mammary Tumor
Prader–willi Syndrome
MAGEL2
Prader–willi Syndrome
SNRPN
Prader–willi Syndrome
KRT17
Pachyonychia Congenita
SSX1
Synovial Sarcoma
SSX2
Synovial Sarcoma
BCL2
Myasthenia Gravis
Huntington's Disease
Synovial Sarcoma
Peripheral Artery Disease
Primary Ovarian Insufficiency
KRT16
Pachyonychia Congenita
PRL
Huntington's Disease
Mammary Tumor
Prader–willi Syndrome
Primary Ovarian Insufficiency
Phobia
TKT
Mammary Tumor
Wernicke Encephalopathy
NFE2L2
Pachyonychia Congenita
Huntington's Disease
Peripheral Artery Disease
Primary Ovarian Insufficiency
SS18
Synovial Sarcoma
FREM1
Trigonocephaly
ACE
Severe Acute Respiratory Syndrome
Huntington's Disease
Synovial Sarcoma
Peripheral Artery Disease
Primary Ovarian Insufficiency
Alexithymia
CAT
Acute Intermittent Porphyria
Huntington's Disease
Phobia
IL6
African Trypanosomiasis
Severe Acute Respiratory Syndrome
Myasthenia Gravis
Huntington's Disease
Bacterial Vaginosis
Synovial Sarcoma
Prader–willi Syndrome
Peripheral Artery Disease
Aneurysm
Primary Ovarian Insufficiency
Alexithymia
ESR1
Severe Acute Respiratory Syndrome
Myasthenia Gravis
Synovial Sarcoma
Mammary Tumor
Primary Ovarian Insufficiency
Alexithymia
Phobia
KRT6A
Pachyonychia Congenita