Disorder of polyamine metabolism
MONDO:0800159An inherited metabolic disease that has its basis in the disruption of the polyamine metabolic process.
1 clinical trial for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Syndromic X-linked intellectual disability Snyder type
(1)
Diaphyseal medullary stenosis-bone malignancy syndrome
(0)
Keratosis follicularis spinulosa decalvans
(0)
Keratosis follicularis spinulosa decalvans, autosomal dominant
(0)
Keratosis follicularis spinulosa decalvans, X-linked
(0)
Neurodevelopmental disorder with alopecia and brain abnormalities
(0)