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.
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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