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MSH: 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.
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umls-label:A18454258,
umls-label:A18798142,
umls-label:A18463447,
umls-label:A18457321,
umls-label:A18799676,
umls-label:A18463448,
umls-label:A18798141,
umls-label:A18469644,
umls-label:A18457322,
umls-label:A18457323,
umls-label:A18457324,
umls-label:A18451166,
umls-label:A18454259,
umls-label:A18804192
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