Concept information
Preferred term
Hyalinosis, Systemic
Type
-
mesh:Descriptor
Definition
- 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.
Broader concept
Entry terms
- 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
Allowable Qualifier(s)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
In other languages
-
French
-
Syndrome de la fibromatose hyaline
URI
http://data.loterre.fr/ark:/67375/JVR-XJ61GNCZ-C
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