Hyalinosis, Systemic

"Hyalinosis, Systemic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

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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. It is comprised of two allelic disorders: infantile systemic hyalinosis and juvenile hyaline fibromatosis. Mutations in the capillary morphogenesis protein-2 are associated with the disorder.

Descriptor ID

D057770

MeSH Number(s)

C16.320.850.368

Concept/Terms

Hyalinosis, Systemic

Juvenile Hyaline Fibromatosis

Infantile Systemic Hyalinosis

Below are MeSH descriptors whose meaning is more general than "Hyalinosis, Systemic".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Skin Diseases, Genetic [C16.320.850]
Hyalinosis, Systemic [C16.320.850.368]

Below are MeSH descriptors whose meaning is related to "Hyalinosis, Systemic".

Below are MeSH descriptors whose meaning is more specific than "Hyalinosis, Systemic".

publications

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