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Diseases
Genes (1272)
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HMBS
Acute Intermittent Porphyria
KRT17
Pachyonychia Congenita
IL6
Acute Pancreatitis
Severe Acute Respiratory Syndrome
African Trypanosomiasis
Callosity
Selenium Deficiency
Peripheral Artery Disease
Cerebral Arteriovenous Malformation
NOTCH3
Cadasil
FREM1
Trigonocephaly
KRT16
Pachyonychia Congenita
Skin Condition
Callosity
G6PD
Hemolytic Anemia
COL4A1
Peripheral Artery Disease
Cadasil
Hemolytic Anemia
KRAS
Hemolytic Anemia
Cerebral Arteriovenous Malformation
Acute Intermittent Porphyria
ACE
Acute Pancreatitis
Severe Acute Respiratory Syndrome
Selenium Deficiency
Peripheral Artery Disease
HMOX1
Acute Pancreatitis
Peripheral Artery Disease
Hemolytic Anemia
TPI1
Hemolytic Anemia
SLC4A1
Hemolytic Anemia
KRT6A
Pachyonychia Congenita
Callosity
BMP2
Callosity
Peripheral Artery Disease
GCLC
Hemolytic Anemia
BMP8A
Peripheral Artery Disease
ITPA
Hemolytic Anemia
SPTB
Hemolytic Anemia
GPI
Hemolytic Anemia