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Diseases
Genes (1558)
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PTPN11
Metachondromatosis
Protein Losing Enteropathy
Cardiofaciocutaneous Syndrome
CHM
Choroideremia
X-Linked Intellectual Disability
MAP2K2
Watson Syndrome
Cardiofaciocutaneous Syndrome
BRAF
Marinesco–sjögren Syndrome
Cardiofaciocutaneous Syndrome
VPS33B
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
PTEN
Proteus-Like Syndrome
Neurological Disorder
Thrombophlebitis
Marinesco–sjögren Syndrome
Protein Losing Enteropathy
MAP2K1
Cardiofaciocutaneous Syndrome
NF1
Fibrous Dysplasia Of Bone
Watson Syndrome
Neurofibromatosis
SNAP29
Cerebral Dysgenesis–neuropathy–ichthyosis–keratoderma Syndrome
VIPAS39
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
GNAS
Fibrous Dysplasia Of Bone
Progressive Osseous Heteroplasia
MYO5A
Griscelli Syndrome
RYR1
Malignant Hyperthermia
KRAS
Marinesco–sjögren Syndrome
Cardiofaciocutaneous Syndrome
RAB3GAP1
Warburg Micro Syndrome 3
Neurological Disorder
MEGF8
Carpenter Syndrome 1
SIL1
Polycystic Liver Disease
Marinesco–sjögren Syndrome
ALS2
Juvenile Primary Lateral Sclerosis
GORAB
Gerodermia Osteodysplastica
RAB23
Carpenter Syndrome 1