Glaucoma 3, primary congenital, d

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Subtype of: Primary congenital glaucoma
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Glaucoma 3, primary congenital, D
EFO_1000968
LTBP2 Causal
19361779 19656777 20179738 20617341 21081970 22025892 22539340
ClinGen, Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Glaucoma 3, primary congenital, d.
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Microspherophakia 1 shared geneLTBP2 Related via 1 shared gene including LTBP2. Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma 1 shared geneLTBP2 Related via 1 shared gene including LTBP2. Congenital keratoglobus 1 shared geneLTBP2 Related via 1 shared gene including LTBP2. Primary congenital glaucoma 1 shared geneLTBP2 Related via 1 shared gene including LTBP2. Weill-marchesani syndrome 1 shared geneLTBP2 Related via 1 shared gene including LTBP2.