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Diseases
Genes (2087)
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TTPA
Visual Impairment
Familial Isolated Vitamin E Deficiency
SLC16A2
Allan-Herndon-Dudley Syndrome
PQBP1
Cataract
Renpenning's Syndrome
UMOD
Medullary Cystic Kidney Disease
PDGFRB
Primary Familial Brain Calcification
Ewing Sarcoma
Rhabdomyosarcoma
SLC20A2
Primary Familial Brain Calcification
SLC4A4
Cataract
Developmental Disability
SLC2A1
Cataract
Developmental Disability
Ewing Sarcoma
Rhabdomyosarcoma
EWSR1
Ewing Sarcoma
Rhabdomyosarcoma
MIP
Cataract
Pleural Effusion
CRYGD
Cataract
SLC33A1
Cataract
Developmental Disability
FLI1
Cataract
Ewing Sarcoma
IFIH1
Singleton Merten Syndrome
RB1
Pinealoblastoma
Cataract
Trilateral Retinoblastoma
Ewing Sarcoma
Rhabdomyosarcoma
LIPA
Acid Lipase Disease
VEGFA
Cataract
Pleural Effusion
Ewing Sarcoma
Rhabdomyosarcoma
PTCH1
Cataract
Ewing Sarcoma
Rhabdomyosarcoma
NBN
Rhabdomyosarcoma
PAX6
Cataract
Visual Impairment