|OBO ID: DOID:0112044|
|Term Name:||non-syndromic X-linked intellectual disability 98||Search Ontology:|
|Definition:||A non-syndromic X-linked intellectual disability characterized by delayed psychomotor development, poor speech, behavioral abnormalities, poor overall growth, dysmorphic facial features, and often early-onset seizures, with males generally more severely affected than females that has_material_basis_in heterozygous or hemizygous mutation in NEXMIF on chromosome Xq13.3. (2)|
|Ontology:||Human Disease (DOID:0112044)|
|is a type of:||
OTHER non-syndromic X-linked intellectual disability 98 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.