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Diseases
Genes (1255)
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PTPN11
Metachondromatosis
Cardiofaciocutaneous Syndrome
Acute Promyelocytic Leukemia
CHM
Choroideremia
X-Linked Intellectual Disability
PQBP1
X-Linked Intellectual Disability
Renpenning's Syndrome
MAP2K2
Watson Syndrome
Cardiofaciocutaneous Syndrome
BRAF
Marinesco–sjögren Syndrome
Cardiofaciocutaneous Syndrome
Acute Promyelocytic Leukemia
VPS33B
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
PMM2
Pmm2 Deficiency
ASL
Argininosuccinic Aciduria
MAP2K1
Cardiofaciocutaneous Syndrome
Acute Promyelocytic Leukemia
TTPA
Familial Isolated Vitamin E Deficiency
VIPAS39
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
SNAP29
Cerebral Dysgenesis–neuropathy–ichthyosis–keratoderma Syndrome
MYO5A
Griscelli Syndrome
RYR1
Malignant Hyperthermia
KRAS
Marinesco–sjögren Syndrome
Cardiofaciocutaneous Syndrome
Acute Promyelocytic Leukemia
RAB3GAP1
Warburg Micro Syndrome 3
GNAS
Progressive Osseous Heteroplasia
PTEN
Proteus-Like Syndrome
Marinesco–sjögren Syndrome
Acute Promyelocytic Leukemia
MEGF8
Carpenter Syndrome 1
NRAS
Cardiofaciocutaneous Syndrome
Acute Promyelocytic Leukemia