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Diseases
Genes (1680)
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PTPN11
Metachondromatosis
Protein Losing Enteropathy
Cardiofaciocutaneous Syndrome
Squamous-Cell Carcinoma Of The Lung
KRAS
Marinesco–sjögren Syndrome
Cardiofaciocutaneous Syndrome
Squamous-Cell Carcinoma Of The Lung
BRAF
Marinesco–sjögren Syndrome
Cardiofaciocutaneous Syndrome
Squamous-Cell Carcinoma Of The Lung
CHM
Choroideremia
X-Linked Intellectual Disability
PQBP1
X-Linked Intellectual Disability
Renpenning's Syndrome
MAP2K2
Watson Syndrome
Cardiofaciocutaneous Syndrome
PTEN
Proteus-Like Syndrome
Thrombophlebitis
Marinesco–sjögren Syndrome
Protein Losing Enteropathy
Squamous-Cell Carcinoma Of The Lung
VPS33B
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
RYR1
Acute Liver Failure
Malignant Hyperthermia
MAP2K1
Cardiofaciocutaneous Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
VIPAS39
Arthrogryposis–renal Dysfunction–cholestasis Syndrome
SNAP29
Cerebral Dysgenesis–neuropathy–ichthyosis–keratoderma Syndrome
GNAS
Fibrous Dysplasia Of Bone
Progressive Osseous Heteroplasia
MYO5A
Griscelli Syndrome
TNFAIP3
Haploinsufficiency Of A20
Acute Liver Failure
NF1
Fibrous Dysplasia Of Bone
Watson Syndrome
Squamous-Cell Carcinoma Of The Lung
RAB3GAP1
Warburg Micro Syndrome 3
MEGF8
Carpenter Syndrome 1
SIL1
Polycystic Liver Disease
Marinesco–sjögren Syndrome