Catalog

15q13.3 deletion

No MMS code

Link to WHO Definition

15q13.3 deletion – http://id.who.int/icd/entity/1824908852

15q13.3 microdeletion (microdel15q13.3) syndrome is characterised by a wide spectrum of neurodevelopmental disorders (developmental delay, mainly in speech acquisition, cognitive impairment, idiopathic generalised epilepsy, neurobehavioural disorders of the autistic or psychotic spectrum), with no or subtle dysmorphic features.

Parents

Proximal deletions of chromosome 15
Syndromic conditions with disorders of intellectual development as a relevant clinical feature