Hyalinosis, Systemic
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.
推出的年份: 2011
树号: C16.320.850.368, C17.800.827.384
MeSH 单一 ID: D057770
进入的组:
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
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