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Human Disease

syndromic X-linked mental retardation Hough type

Term ID
DOID:0080242
Synonyms
Definition
A syndromic X-linked intellectual disability that is characterized by delayed development, intellectual disability, speech and language delay, and early-onset seizures and that has_material_basis_in hemizygous or heterozygous mutation in the CNKSR2 gene on chromosome Xp22. https://pubmed.ncbi.nlm.nih.gov/28098945/
References
Ontology
Human Disease   ( DOID:0080242 )
Relationships
is a type of
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Genes Involved
Zebrafish Models