< Back

Mucinoses

Categorical breakdown of terms falling inder the category of Mucinoses. Sub categories will become more specific in nature to the terms listed for Mucinoses.

Sub-Categories

Terms

Ganglion Cysts - Nodular tumor-like lesions or mucoid flesh, arising from tendon sheaths, LIGAMENTS, or JOINT CAPSULE...

Mucinoses - Mucoid states characterized by the elevated deposition and accumulation of mucin (mucopolysaccharide...

Mucinosis, Follicular - A disease of the pilosebaceous unit, presenting clinically as grouped follicular papules or plaques ...

Mucopolysaccharidoses - Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in ...

Mucopolysaccharidosis I - Systemic lysosomal storage disease caused by a deficiency of alpha-L-iduronidase (IDURONIDASE) and c...

Mucopolysaccharidosis II - Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a defi...

Mucopolysaccharidosis III - Mucopolysaccharidosis characterized by heparitin sulfate in the urine, progressive mental retardatio...

Mucopolysaccharidosis IV - Genetic disorder of mucopolysaccharide metabolism characterized by skeletal abnormalities, joint ins...

Mucopolysaccharidosis VI - Mucopolysaccharidosis with excessive chondroitin sulfate B in urine, characterized by dwarfism and d...

Mucopolysaccharidosis VII - Mucopolysaccharidosis characterized by excessive dermatan and heparan sulfates in the urine and Hurl...

Myxedema - A condition characterized by a dry, waxy type of swelling (EDEMA) with abnormal deposits of MUCOPOLY...

Scleredema Adultorum - A diffuse, non-pitting induration of the skin of unknown etiology that occurs most commonly in assoc...

Scleromyxedema - A connective tissue disorder characterized by widespread thickening of SKIN with a cobblestone-like ...