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Human Disease

non-syndromic X-linked intellectual disability 99

Term ID
DOID:0112026
Synonyms
  • MRX99
  • X-linked mental retardation 99
Definition
A non-syndromic X-linked intellectual disability characterized by developmental delay, hypotonia, and variable behavioral abnormalities that has_material_basis_in hemizygous mutation in the USP9X gene on chromosome Xp11.4. https://pubmed.ncbi.nlm.nih.gov/24607389/
References
Ontology
Human Disease   ( DOID:0112026 )
Relationships
is a type of
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Genes Involved
Zebrafish Models