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Diseases
Genes (726)
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MYO5A
Griscelli Syndrome
Griscelli Syndrome
PTPN11
Metachondromatosis
Protein Losing Enteropathy
Cardiofaciocutaneous Syndrome
CHM
Choroideremia
MAP2K2
Watson Syndrome
Cardiofaciocutaneous Syndrome
BRAF
Marinesco–sjögren Syndrome
Cardiofaciocutaneous Syndrome
VPS33B
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
PTEN
Proteus-Like Syndrome
Membranoproliferative Glomerulonephritis
Thrombophlebitis
Marinesco–sjögren Syndrome
Protein Losing Enteropathy
SLC12A6
Andermann Syndrome
MAP2K1
Cardiofaciocutaneous Syndrome
VIPAS39
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
GNAS
Fibrous Dysplasia Of Bone
Progressive Osseous Heteroplasia
SNAP29
Cerebral Dysgenesis–neuropathy–ichthyosis–keratoderma Syndrome
RYR1
Malignant Hyperthermia
RAB3GAP1
Warburg Micro Syndrome 3
KRAS
Marinesco–sjögren Syndrome
Cardiofaciocutaneous Syndrome
MEGF8
Carpenter Syndrome 1
SIL1
Polycystic Liver Disease
Marinesco–sjögren Syndrome
NF1
Fibrous Dysplasia Of Bone
Watson Syndrome
ALS2
Juvenile Primary Lateral Sclerosis
GORAB
Gerodermia Osteodysplastica