Cutis laxa, autosomal dominant 3

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Subtype of: Cutis laxa
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Cutis laxa, autosomal dominant 3
MONDO_0014706
ALDH18A1 Causal
18388779 26320891 24767728 24913064 11092761 18478038 21739576 27604308 22170564 24816252 29903433 26297558 28228640 26829900 26297557 26026163
Open Targets
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Cutis laxa, autosomal dominant 3.
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De barsy syndrome 1 shared geneALDH18A1 Related via 1 shared gene including ALDH18A1. P5CS deficiency 1 shared geneALDH18A1 Related via 1 shared gene including ALDH18A1. Developmental disorder-joint hypermobility-skin laxity with or without metabolic abnormalities 1 shared geneALDH18A1 Related via 1 shared gene including ALDH18A1. Cutis laxa, corneal clouding, and mental retardation 1 shared geneALDH18A1 Related via 1 shared gene including ALDH18A1. Cutis laxa, autosomal recessive, 3a 1 shared geneALDH18A1 Related via 1 shared gene including ALDH18A1.