Congenital membranous nephropathy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL MEMBRANOUS NEPHROPATHY DUE TO FETOMATERNAL ANTI-NEUTRAL ENDOPEPTIDASE ALLOIMMUNIZATION
69063
MME Unknown
15464186
Orphanet
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Congenital membranous nephropathy.
5 View disease cluster →
Charcot-Marie-Tooth disease type 2T 1 shared geneMME Related via 1 shared gene including MME. Cryopyrin-associated periodic syndrome 1 shared geneMME Related via 1 shared gene including MME. Membranous glomerulonephritis 1 shared geneMME Related via 1 shared gene including MME. Dejerine-sottas disease 1 shared geneMME Related via 1 shared gene including MME. Hypertrophic neuropathy 1 shared geneMME Related via 1 shared gene including MME.