Diseases

Hyaline Fibromatosis Syndrome

Autosomal recessive disorder characterized by HYALINE deposition in the skin, bone, gastrointestinal tract, muscles and glands; multiple subcutaneous skin nodules; GINGIVAL HYPERTROPHY; and joint CONTRACTURES. Mutations in the capillary morphogenesis protein-2 are associated with the disorder.

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

Autosomal recessive disorder characterized by HYALINE deposition in the skin, bone, gastrointestinal tract, muscles and glands; multiple subcutaneous skin nodules; GINGIVAL HYPERTROPHY; and joint CONTRACTURES. Mutations in the capillary morphogenesis protein-2 are associated with the disorder.

MeSH Record

Classification

Broader headings

Related Concepts

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MeSH Record

See Also

MeSH Record

Synonyms

38 entry terms
  • Fibromatosis Hyalinica Multiplex Juvenilis
  • Fibromatosis Juvenile Hyaline
  • Fibromatosis, Juvenile Hyaline
  • Hyaline Fibromatosis Juvenile
  • Hyalinosis, Systemic
  • Hyalinosis, Systemic Juvenile
  • Juvenile Hyaline Fibromatosis
  • Juvenile Hyalinosis
  • Murray Syndrome
  • Puretic Syndrome
  • Systemic Hyalinosis
  • Fibromatosis Syndrome, Hyaline
  • Fibromatosis Syndromes, Hyaline
  • Hyaline Fibromatosis Syndromes
  • Hyaline Fibromatosis, Juvenile
  • Hyalinoses, Juvenile
  • Hyalinoses, Systemic
  • Hyalinoses, Systemic Juvenile
  • Hyalinosis, Juvenile
  • Juvenile Hyaline Fibromatoses
  • Juvenile Hyalinoses
  • Juvenile Hyalinoses, Systemic
  • Juvenile Hyalinosis, Systemic
  • Puretic Syndromes
  • Syndrome, Hyaline Fibromatosis
  • Syndrome, Murray
  • Syndrome, Puretic
  • Syndromes, Hyaline Fibromatosis
  • Syndromes, Puretic
  • Systemic Hyalinoses
  • Systemic Juvenile Hyalinoses
  • Systemic Juvenile Hyalinosis
  • Infantile Systemic Hyalinosis
  • Hyalinoses, Infantile Systemic
  • Hyalinosis, Infantile Systemic
  • Infantile Systemic Hyalinoses
  • Systemic Hyalinoses, Infantile
  • Systemic Hyalinosis, Infantile

MeSH Record

Aspects Covered

34 allowable subheadings

Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.

MeSH Record

Indexing Annotation

do not confuse entry term INFANTILE SYSTEMIC HYALINOSIS with HYALINE MEMBRANE DISEASE

MeSH Record

History Note

2011

MeSH Record

Previous Indexing

  • Hyalin (1975-2010)

MeSH Hierarchy

Tree Numbers

  1. C16w.320w.850w.368w
  2. C17.800w.827w.384w

AMA Style

References

  1. National Library of Medicine. Hyaline Fibromatosis Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D057770. http://id.nlm.nih.gov/mesh/2026/D057770
  2. Hyaline Fibromatosis Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Infantile_systemic_hyalinosis
  3. Hyaline Fibromatosis Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q6029067