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.

Descriptor ID	D057770
MeSH Number(s)	C16.320.850.368 C17.800.827.384
Concept/Terms	Hyalinosis, Systemic Hyalinosis, Systemic Hyalinoses, Systemic Systemic Hyalinoses Systemic Hyalinosis Infantile Systemic Hyalinosis Hyalinoses, Infantile Systemic Hyalinosis, Infantile Systemic Infantile Systemic Hyalinoses Systemic Hyalinoses, Infantile Systemic Hyalinosis, Infantile Juvenile Hyaline Fibromatosis Fibromatosis Hyalinica Multiplex Juvenilis Murray Syndrome Syndrome, Murray Hyaline Fibromatosis Juvenile Fibromatosis, Juvenile Hyaline Hyaline Fibromatosis, Juvenile Juvenile Hyaline Fibromatoses Hyalinosis, Systemic Juvenile Hyalinoses, Systemic Juvenile Juvenile Hyalinoses, Systemic Juvenile Hyalinosis, Systemic Systemic Juvenile Hyalinoses Systemic Juvenile Hyalinosis Puretic Syndrome Puretic Syndromes Syndrome, Puretic Syndromes, Puretic Juvenile Hyalinosis Hyalinoses, Juvenile Hyalinosis, Juvenile Juvenile Hyalinoses Hyaline Fibromatosis Syndrome Fibromatosis Syndrome, Hyaline Fibromatosis Syndromes, Hyaline Hyaline Fibromatosis Syndromes Syndrome, Hyaline Fibromatosis Syndromes, Hyaline Fibromatosis Fibromatosis Juvenile Hyaline

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

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

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