Seckel syndrome 10

Definition

Any Seckel syndrome in which the cause of the disease is a mutation in the NSMCE2 gene.

Also known as NSMCE2 Seckel syndrome, SCKL10, Seckel syndrome 10, Seckel syndrome caused by mutation in NSMCE2, Seckel syndrome type 10 — per MONDO

Also identified as

• DOID 0070008 per MONDO
• OMIM 617253 per MONDO
• UMLS C4310647 per MONDO