autosomal recessive cutis laxa type IB

Summary
Synonym
  • ARCL1B
Definition
An autosomal recessive cutis laxa type I characterized by disturbed elastic fiber formation resulting in severe systemic connective tissue abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the EFEMP2 gene on chromosome 11q13.
Super Class
autosomal recessive cutis laxa type I
Disease Ontology
DOID:0070133
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
30008 EFEMP2 EGF containing fibulin extracellular matrix protein 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
58859 Efemp2 epidermal growth factor-containing fibulin-like extracellular matrix protein 2

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024