Mucolipidosis type III, alpha/beta

MONDO:0018931

Mucolipidosis III alpha/beta (MLIII alpha/beta) is a lysosomal disorder characterized by progressive slowing of the growth rate from early childhood, stiffness and pain in joints, gradual coarsening of facial features, moderate developmental delay and mild intellectual disability in most patients.

Also known as: ML 3, ML3, mucolipidosis 3, mucolipidosis III, ML 3 alpha/beta, ML III alpha/beta, MLIII, Pseudo Hurler Polydystrophy

0 clinical trials for this condition and its sub-types, 0 tagged with Mucolipidosis type III, alpha/beta itself.

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↑ Lysosomal storage disease with skeletal involvement (63) ↑ Familial mucolipidosis (5) ↑ GNPTAB-mucolipidosis (0)

Including sub-types (0) Tagged with Mucolipidosis type III, alpha/beta (0)

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