An inherited metabolic disease that has its basis in the disruption of the polyamine metabolic process.
Comprehensive, easy-to-understand information about this condition
Checking for content...
No external resources available.
keratosis follicularis spinulosa decalvans
MONDO:0000136
diaphyseal medullary stenosis-bone malignancy syndrome
MONDO:0007205
syndromic X-linked intellectual disability Snyder type
MONDO:0010664
inborn disorder of peptide metabolism
MONDO:0019232
neurodevelopmental disorder with alopecia and brain abnormalities
MONDO:0033642
inherited glutathione metabolism disease
MONDO:0040566