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Diseases
Genes (1444)
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PTPN11
Acute Promyelocytic Leukemia
Metachondromatosis
Cardiofaciocutaneous Syndrome
CHM
Choroideremia
BRAF
Acute Promyelocytic Leukemia
Marinesco–sjögren Syndrome
Vascular Malformation
Cardiofaciocutaneous Syndrome
MAP2K2
Watson Syndrome
Cardiofaciocutaneous Syndrome
VPS33B
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
ASL
Argininosuccinic Aciduria
TBX5
Holt–oram Syndrome
PMM2
Pmm2 Deficiency
IFT140
Short-Rib Thoracic Dysplasia 9 With Or Without Polydactyly
Marinesco–sjögren Syndrome
MAP2K1
Acute Promyelocytic Leukemia
Cardiofaciocutaneous Syndrome
SLC6A19
Hartnup Disease
VIPAS39
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
SNAP29
Cerebral Dysgenesis–neuropathy–ichthyosis–keratoderma Syndrome
MYO5A
Griscelli Syndrome
MARS2
Spastic Ataxia 3, Autosomal Recessive
KRAS
Acute Promyelocytic Leukemia
Marinesco–sjögren Syndrome
Cardiofaciocutaneous Syndrome
NPC1
Niemann–pick Disease, Type C
RAB3GAP1
Warburg Micro Syndrome 3
NRAS
Acute Promyelocytic Leukemia
Cardiofaciocutaneous Syndrome
PTEN
Acute Promyelocytic Leukemia
Proteus-Like Syndrome
Marinesco–sjögren Syndrome
Vascular Malformation