Cutis laxa, autosomal recessive, type ia

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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, type IA
MONDO_0009052
FBLN5 Unknown
11805835 27089918 11805834 12189163 16153447 22829427 12618961 23328402 20301756
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Cutis laxa, autosomal recessive, type ia.
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Cutis laxa, autosomal recessive, 1a 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.