/neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy

neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy

MONDO:0859266

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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