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Diseases
Genes (2878)
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KANK2
Neuroblastoma, Susceptibility To, 7
Palmoplantar Keratoderma And Woolly Hair
Nephrotic Syndrome, Type 16
ST3GAL3
Epileptic Encephalopathy, Early Infantile, 15
Mental Retardation, Autosomal Recessive 12
PMM2
Pmm2 Deficiency
Epileptic Encephalopathy, Early Infantile, 15
SLC6A19
Hartnup Disease
ASL
Argininosuccinic Aciduria
COMP
Pseudoachondroplasia
PAX6
Aniridia 3
SCNN1B
Liddle Syndrome 2
KERA
Cornea Plana 2, Autosomal Recessive
VCP
Inclusion Body Myopathy With Early-Onset Paget Disease With Or Without Frontotemporal Dementia 3
LIN28B
Neuroblastoma, Susceptibility To, 7
RBM8A
Thrombocytopenia-Absent Radius Syndrome
NTRK2
Epileptic Encephalopathy, Early Infantile, 15
Neuroblastoma, Susceptibility To, 7
AHDC1
Xia–gibbs Syndrome
PHOX2B
Pinealoblastoma
Neuroblastoma, Susceptibility To, 7
MKS1
Bardet-Biedl Syndrome 11
SAMD9
Tumoral Calcinosis, Normophosphatemic, Familial
SAMD9L
Ataxia-Pancytopenia Syndrome
CRYBB3
Cataract 22, Multiple Types
MYCN
Pinealoblastoma
Trilateral Retinoblastoma
Neuroblastoma, Susceptibility To, 7