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Diseases
Genes (682)
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KANK2
Nephrotic Syndrome, Type 16
Palmoplantar Keratoderma And Woolly Hair
KRT1
Keratosis Palmoplantaris Striata Iii
Ichthyosis, Cyclic, With Epidermolytic Hyperkeratosis
ST3GAL3
Epileptic Encephalopathy, Early Infantile, 15
Mental Retardation, Autosomal Recessive 12
COMP
Pseudoachondroplasia
SCNN1B
Liddle Syndrome 2
PAX6
Aniridia 3
SOS1
Epileptic Encephalopathy, Early Infantile, 15
Noonan Syndrome 5
PTPN11
Chromosome 8p11 Myeloproliferative Syndrome
Noonan Syndrome 5
KERA
Cornea Plana 2, Autosomal Recessive
CXCR4
Whim Syndrome
RAF1
Noonan Syndrome 5
KRAS
Noonan Syndrome 5
TFAP2B
Char Syndrome
VCP
Inclusion Body Myopathy With Early-Onset Paget Disease With Or Without Frontotemporal Dementia 3
RBM8A
Thrombocytopenia-Absent Radius Syndrome
LZTR1
Noonan Syndrome 5
RIT1
Noonan Syndrome 5
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