Disorder

Connective Tissue Diseases

AMW:DIS:170002

A heterogeneous group of disorders, some hereditary, others acquired, characterized by abnormal structure or function of one or more of the elements of connective tissue, i.e., collagen, elastin, or the mucopolysaccharides.

Pathology clinical

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Cellulitis has parent Connective Tissue Diseases

Neoplasms, Connective Tissue has parent Connective Tissue Diseases

Dupuytren Contracture has parent Connective Tissue Diseases

Fibromatosis, Plantar has parent Connective Tissue Diseases

Weill-Marchesani Syndrome has parent Connective Tissue Diseases

Marfan Syndrome has parent Connective Tissue Diseases

Osteopoikilosis has parent Connective Tissue Diseases

Cartilage Diseases has parent Connective Tissue Diseases

Dermatomyositis has parent Connective Tissue Diseases

Noonan Syndrome has parent Connective Tissue Diseases

Rheumatic Diseases has parent Connective Tissue Diseases

Homocystinuria has parent Connective Tissue Diseases

Penile Induration has parent Connective Tissue Diseases

Pseudoxanthoma Elasticum has parent Connective Tissue Diseases

Cutis Laxa has parent Connective Tissue Diseases

Anetoderma has parent Connective Tissue Diseases

Collagen Diseases has parent Connective Tissue Diseases

Lipedema has parent Connective Tissue Diseases

Lupus Erythematosus, Cutaneous has parent Connective Tissue Diseases

Lupus Erythematosus, Systemic has parent Connective Tissue Diseases

Mixed Connective Tissue Disease has parent Connective Tissue Diseases

Mucinoses has parent Connective Tissue Diseases

Panniculitis has parent Connective Tissue Diseases

Scleroderma, Localized has parent Connective Tissue Diseases

Scleroderma, Systemic has parent Connective Tissue Diseases

Undifferentiated Connective Tissue Diseases has parent Connective Tissue Diseases

Connective Tissue Diseases has parent Skin and Connective Tissue Diseases

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