hyaline fibromatosis syndrome

Summary
Synonym
  • HFS
  • inherited systemic hyalinosis
  • puretic syndrome
  • systemic hyalinosis
Definition
A connective tissue disease characterized by abnormal growth of hyalinized fibrous tissue especially around the subcutaneous regions on the scalp, ears, neck, face, hands, and feet, gingival hypertrophy, joint contractures, and osteolytic bone lesions that has_material_basis_in homozygous or compound heterozygous mutation in the ANTXR2 gene on chromosome 4q21.21.
Super Class
autosomal recessive disease connective tissue disease
Disease Ontology
DOID:0111669
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
118429 ANTXR2 ANTXR cell adhesion molecule 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
71914 Antxr2 anthrax toxin receptor 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