MeSH Browser

MeSH Heading: Hyaline Fibromatosis Syndrome
Tree Number(s): C16.320.850.368; C17.800.827.384
Unique ID: D057770
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D057770
Annotation: do not confuse entry term INFANTILE SYSTEMIC HYALINOSIS with HYALINE MEMBRANE DISEASE
Scope Note: 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.
Entry Term(s): Fibromatosis Hyalinica Multiplex Juvenilis; Fibromatosis Juvenile Hyaline; Fibromatosis, Juvenile Hyaline; Hyaline Fibromatosis Juvenile; Hyalinosis, Systemic; Hyalinosis, Systemic Juvenile; Infantile Systemic Hyalinosis; Juvenile Hyaline Fibromatosis; Juvenile Hyalinosis; Murray Syndrome; Puretic Syndrome; Systemic Hyalinosis
Previous Indexing: Hyalin (1975-2010)
See Also: Hyaline Membrane Disease; Lipoid Proteinosis of Urbach and Wiethe
Public MeSH Note: 2011
History Note: 2011
Date Established: 2011/01/01
Date of Entry: 2010/06/25
Revision Date: 2023/08/25

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Skin Diseases, Genetic [C16.320.850]

Skin and Connective Tissue Diseases [C17]
- Skin Diseases [C17.800]
  - Skin Diseases, Genetic [C17.800.827]

Hyaline Fibromatosis Syndrome Preferred

Concept UI: M0539002
Scope Note: 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.
Terms: Hyaline Fibromatosis Syndrome Preferred Term
Term UI T757582
Date09/11/2009
LexicalTag NON
ThesaurusID NLM (2011); Puretic Syndrome
Term UI T801796
Date11/15/2011
LexicalTag NON
ThesaurusID; Juvenile Hyalinosis
Term UI T841795
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Murray Syndrome
Term UI T841797
Date04/18/2013
LexicalTag EPO
ThesaurusID GHR (2014); Hyalinosis, Systemic
Term UI T757581
Date09/11/2009
LexicalTag NON
ThesaurusID NLM (2011); Systemic Hyalinosis
Term UI T757583
Date09/11/2009
LexicalTag NON
ThesaurusID; Juvenile Hyaline Fibromatosis
Term UI T757585
Date09/11/2009
LexicalTag NON
ThesaurusID; Fibromatosis Hyalinica Multiplex Juvenilis
Term UI T757586
Date09/11/2009
LexicalTag NON
ThesaurusID NLM (2011); Fibromatosis Juvenile Hyaline
Term UI T757587
Date09/11/2009
LexicalTag NON
ThesaurusID; Hyaline Fibromatosis Juvenile
Term UI T757588
Date09/11/2009
LexicalTag NON
ThesaurusID; Hyalinosis, Systemic Juvenile
Term UI T801795
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Fibromatosis, Juvenile Hyaline
Term UI T801794
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013)

Infantile Systemic Hyalinosis Narrower

Hyaline Fibromatosis Syndrome MeSH Descriptor Data 2025