Cutis laxa, autosomal recessive, 1a

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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 recessive, 1A
MONDO_0009052
FBLN5 Unknown
20599547 17035250 12189163 16691202 18185537 16652333 20007835 21576112
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Cutis laxa, autosomal recessive, 1a.
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Cutis laxa, autosomal recessive, type ia 1 shared geneFBLN5 Related via 1 shared gene including FBLN5. Cutis laxa, autosomal dominant, 2 1 shared geneFBLN5 Related via 1 shared gene including FBLN5. Demyelinating hereditary motor and sensory neuropathy 1 shared geneFBLN5 Related via 1 shared gene including FBLN5. Proximal spinal muscular atrophy 1 shared geneFBLN5 Related via 1 shared gene including FBLN5. Accessory skin tag 1 shared geneFBLN5 Related via 1 shared gene including FBLN5.