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Diseases
Genes (1428)
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COL2A1
Collagen, Type Ii, Alpha-1
Cataract
GJA1
Oculodentodigital Dysplasia
Cataract
AFG3L2
Spinocerebellar Ataxia Type 28
TTPA
Familial Isolated Vitamin E Deficiency
FOXP3
Ipex Syndrome
PQBP1
Cataract
Renpenning's Syndrome
PRPS1
Arts Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
Bronchopulmonary Dysplasia
CRYGD
Cataract
MIP
Cataract
PAH
Cataract
Phenylketonuria
IFIH1
Singleton Merten Syndrome
TGM1
Bathing Suit Ichthyosis
HLA-DRB1
Eosinophilia–myalgia Syndrome
Cataract
Giant Cell Arteritis
PDGFB
Primary Familial Brain Calcification
RB1
Pinealoblastoma
Cataract
Trilateral Retinoblastoma
CRYAA
Cataract
PITX3
Cataract
CRYAB
Cataract