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Metadata
ID	DOID:0080737
Name	Ehlers-Danlos syndrome musculocontractural type 2
Definition	An Ehlers-Danlos syndrome that is characterized by progressive multisystem fragility-related manifestations, including joint dislocations and deformities; skin hyperextensibility, bruisability, and fragility, with recurrent large subcutaneous hematomas; cardiac valvular, respiratory, gastrointestinal, and ophthalmologic complications; and myopathy, featuring muscle hypoplasia, muscle weakness, and an abnormal muscle fiber pattern in histology in adulthood, resulting in gross motor developmental delay and that has_material_basis_in homozygous mutation in the DSE gene on chromosome 6q22. https://pubmed.ncbi.nlm.nih.gov/28306229/
Xrefs	MIM:615539
Parent Relationships	is_a Ehlers-Danlos syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance has symptom some muscle weakness