/neurodevelopmental disorder with microcephaly and movement abnormalities

neurodevelopmental disorder with microcephaly and movement abnormalities

MONDO:0957531

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

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

microcephaly and chorioretinopathy

MONDO:0000181

microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability

MONDO:0007918

autosomal dominant primary microcephaly

MONDO:0007988

Prader-Willi syndrome

MONDO:0008300

Smith-Magenis syndrome

MONDO:0008434

microcephalic osteodysplastic primordial dwarfism type I

MONDO:0008871