Aminoacylase deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
AMINOACYLASE 1 DEFICIENCY
C1835922
ABHD14A-ACY1 Unknown — Disgenet
ZNF335 Unknown — Disgenet —
AMINOACYLASE DEFICIENCY
C5681074
ABHD14A-ACY1 Unknown — Disgenet
ACY1 Unknown — Disgenet
All4 Causal2 Unknown3
Related Diseases Diseases that share the most curated genes with Aminoacylase deficiency.
5 View disease cluster →
Becker nevus syndrome 1 shared geneACTB Related via 1 shared gene including ACTB. Congenital smooth muscle hamartoma 1 shared geneACTB Related via 1 shared gene including ACTB. Developmental malformations-deafness-dystonia syndrome 1 shared geneACTB Related via 1 shared gene including ACTB. Dystonia-deafness syndrome 1 shared geneACTB Related via 1 shared gene including ACTB. ACTB-associated syndromic thrombocytopenia 1 shared geneACTB Related via 1 shared gene including ACTB.