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Diseases
Genes (691)
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PTPN11
Metachondromatosis
Protein Losing Enteropathy
Cardiofaciocutaneous Syndrome
PTEN
Chorangioma
Proteus-Like Syndrome
Thrombophlebitis
Marinesco–sjögren Syndrome
Protein Losing Enteropathy
PQBP1
X-Linked Intellectual Disability
Renpenning's Syndrome
CHM
Choroideremia
X-Linked Intellectual Disability
MAP2K2
Watson Syndrome
Cardiofaciocutaneous Syndrome
BRAF
Marinesco–sjögren Syndrome
Cardiofaciocutaneous Syndrome
VPS33B
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
MAP2K1
Cardiofaciocutaneous Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
SNAP29
Cerebral Dysgenesis–neuropathy–ichthyosis–keratoderma Syndrome
VIPAS39
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
GNAS
Fibrous Dysplasia Of Bone
Progressive Osseous Heteroplasia
MYO5A
Griscelli Syndrome
KRAS
Marinesco–sjögren Syndrome
Cardiofaciocutaneous Syndrome
RAB3GAP1
Warburg Micro Syndrome 3
MEGF8
Carpenter Syndrome 1
SIL1
Polycystic Liver Disease
Marinesco–sjögren Syndrome
GORAB
Gerodermia Osteodysplastica
ALS2
Juvenile Primary Lateral Sclerosis
NF1
Fibrous Dysplasia Of Bone
Watson Syndrome