/Seckel syndrome 10

Seckel syndrome 10

Rare Disease

MONDO:0014991

Also Known As

NSMCE2 Seckel syndromeSCKL10Seckel syndrome 10Seckel syndrome caused by mutation in NSMCE2Seckel syndrome type 10

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

Comprehensive, easy-to-understand information about this condition

Checking for content...

Gene data from MyGene.info • Click to view on NCBI Gene

Seckel syndrome 1

MONDO:0008869

microcephalic osteodysplastic primordial dwarfism type II

MONDO:0008872

Lowry-Wood syndrome

MONDO:0009191

Hallermann-Streiff syndrome

MONDO:0009318

hypoparathyroidism-retardation-dysmorphism syndrome

MONDO:0009426

microcephalic primordial dwarfism, Toriello type

MONDO:0009616