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Diseases NameMondo IDAssociated TargetsDirect Associated TargetsRare
CystathioninuriaMONDO:0009058
Pilarowski-Bjornsson syndromeMONDO:0060568
Microcephaly 22, primary, autosomal recessiveMONDO:0054805
Cone dystrophy, retinal 3A
Retinitis pigmentosa 57MONDO:0013315
Alport syndrome, autosomal recessive
Hematuria, benign familialMONDO:0007709
Alport syndrome, autosomal dominant
Complement component 2 deficiencyMONDO:0009006
Ehlers-Danlos syndrome, vascular typeMONDO:0017314