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.
Year introduced: 2011
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Subheadings:
Tree Number(s): C16.320.850.368, C17.800.827.384
MeSH Unique ID: D057770
Entry Terms:
- Fibromatosis Syndrome, Hyaline
- Fibromatosis Syndromes, Hyaline
- Hyaline Fibromatosis Syndromes
- Syndrome, Hyaline Fibromatosis
- Syndromes, Hyaline Fibromatosis
- Puretic Syndrome
- Puretic Syndromes
- Syndrome, Puretic
- Syndromes, Puretic
- Juvenile Hyalinosis
- Hyalinoses, Juvenile
- Hyalinosis, Juvenile
- Juvenile Hyalinoses
- Murray Syndrome
- Syndrome, Murray
- Hyalinosis, Systemic
- Hyalinoses, Systemic
- Systemic Hyalinoses
- Systemic Hyalinosis
- Juvenile Hyaline Fibromatosis
- Hyaline Fibromatosis, Juvenile
- Juvenile Hyaline Fibromatoses
- Fibromatosis Hyalinica Multiplex Juvenilis
- Fibromatosis Juvenile Hyaline
- Hyaline Fibromatosis Juvenile
- Hyalinosis, Systemic Juvenile
- Hyalinoses, Systemic Juvenile
- Juvenile Hyalinoses, Systemic
- Juvenile Hyalinosis, Systemic
- Systemic Juvenile Hyalinoses
- Systemic Juvenile Hyalinosis
- Fibromatosis, Juvenile Hyaline
- Infantile Systemic Hyalinosis
- Hyalinoses, Infantile Systemic
- Hyalinosis, Infantile Systemic
- Infantile Systemic Hyalinoses
- Systemic Hyalinoses, Infantile
- Systemic Hyalinosis, Infantile
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