Category:Pseudoxanthoma elasticum

**inherited pseudoxanthoma elasticum**
	Human disease
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Instance of	designated intractable/rare disease; developmental defect during embryogenesis; rare disease; class of disease;
Subclass of	autosomal recessive disease; connective tissue disease; genetic central nervous system and retinal vascular disease; central nervous system and retinal vascular disease; dermis elastic tissue disorder; familial restrictive cardiomyopathy; connective tissue disease with eye involvement; malformation syndrome with skin/mucosae involvement; rare developmental defect with connective tissue involvement; inherited or acquired pseudoxanthoma elasticum; genetic hypertension;
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	Q1052391;
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Media in category "Pseudoxanthoma elasticum"

The following 3 files are in this category, out of 3 total.