Aplasia cutis congenita

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
APLASIA CUTIS CONGENITA
1114C0282160HP:0001057MONDO:0007145
BMS1 Causal
23785305
ClinVar, Disgenet, GWAS catalog, Orphanet
All5 Causal1 Unknown5
Related Diseases Diseases that share the most curated genes with Aplasia cutis congenita.
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Other epidermolysis bullosa 2 shared genesPLEC, ITGB4 Related via 2 shared genes including PLEC, ITGB4. Acces syndrome 1 shared geneUBA2 Related via 1 shared gene including UBA2. Chromosome 19q13.11 deletion syndrome 1 shared geneUBA2 Related via 1 shared gene including UBA2. Epidermolysa bullosa simplex and limb girdle muscular dystrophy 1 shared genePLEC Related via 1 shared gene including PLEC. PLEC-related muscular dystrophy-epidermolysis bullosa simplex spectrum disorder 1 shared genePLEC Related via 1 shared gene including PLEC.