Disorder of polyamine metabolism

rare

An inherited metabolic disease that has its basis in the disruption of the polyamine metabolic process.

Subtypes

Disease	ID	Subtypes	Genes
Keratosis follicularis spinulosa decalvans	MONDO:0000136	2
Diaphyseal medullary stenosis-bone malignancy syndrome	MONDO:0007205		MTAP
Neurodevelopmental disorder with alopecia and brain abnormalities	MONDO:0033642		ODC1
Syndromic X-linked intellectual disability Snyder type	MONDO:0010664		SMS

Rare disease

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