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Diseases
Genes (2806)
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ST3GAL3
Epileptic Encephalopathy, Early Infantile, 15
Mental Retardation, Autosomal Recessive 12
COMP
Pseudoachondroplasia
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
LIN28B
Neuroblastoma, Susceptibility To, 7
RBM8A
Thrombocytopenia-Absent Radius Syndrome
NTRK2
Epileptic Encephalopathy, Early Infantile, 15
Neuroblastoma, Susceptibility To, 7
PHOX2B
Pinealoblastoma
Neuroblastoma, Susceptibility To, 7
NR2F1
Epileptic Encephalopathy, Early Infantile, 15
Bosch-Boonstra-Schaaf Optic Atrophy Syndrome
AHDC1
Xia–gibbs Syndrome
MKS1
Bardet-Biedl Syndrome 11
SAMD9L
Ataxia-Pancytopenia Syndrome
SAMD9
Tumoral Calcinosis, Normophosphatemic, Familial
CRYBB3
Cataract 22, Multiple Types
MYCN
Pinealoblastoma
Neuroblastoma, Susceptibility To, 7
COL2A1
Pseudoachondroplasia
Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness
BBS10
Bardet-Biedl Syndrome 11
ALK
Neuroblastoma, Susceptibility To, 7
LMO1
Neuroblastoma, Susceptibility To, 7