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Hyalinosis, Systemic MeSH Descriptor Data 2021


MeSH Heading
Hyalinosis, Systemic
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
Hyaline Fibromatosis Syndrome
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
2015/06/18
Hyalinosis, Systemic Preferred
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