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Diseases
Genes (574)
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KANK2
Nephrotic Syndrome, Type 16
Palmoplantar Keratoderma And Woolly Hair
ST3GAL3
Epileptic Encephalopathy, Early Infantile, 15
Mental Retardation, Autosomal Recessive 12
COMP
Pseudoachondroplasia
PAX6
Aniridia 3
SOS1
Epileptic Encephalopathy, Early Infantile, 15
Noonan Syndrome 5
PTPN11
Chromosome 8p11 Myeloproliferative Syndrome
Noonan Syndrome 5
CXCR4
Whim Syndrome
RAF1
Noonan Syndrome 5
KRAS
Noonan Syndrome 5
TFAP2B
Char Syndrome
KERA
Cornea Plana 2, Autosomal Recessive
SCNN1B
Liddle Syndrome 2
VCP
Inclusion Body Myopathy With Early-Onset Paget Disease With Or Without Frontotemporal Dementia 3
LZTR1
Noonan Syndrome 5
RIT1
Noonan Syndrome 5
RBM8A
Thrombocytopenia-Absent Radius Syndrome
AHDC1
Xia–gibbs Syndrome
SHOC2
Inclusion Body Myopathy With Early-Onset Paget Disease With Or Without Frontotemporal Dementia 3
Noonan Syndrome 5
SCN9A
Paroxysmal Extreme Pain Disorder
KMT2A
Lysine-Specific Methyltransferase 2a