Search Ontology:
Human Disease
X-linked intellectual developmental disorder 108
- Term ID
- DOID:0111844
- Synonyms
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- MRX108
- Definition
- A syndromic X-linked intellectual disability characterized by global developmental delay, delayed walking, and poor speech acquisition that has_material_basis_in hemizygous mutation in the SLC9A7 gene on chromosome Xp11.3. https://www.ncbi.nlm.nih.gov/pubmed/30335141
- References
- Ontology
- Human Disease ( DOID:0111844 )
- is a type of
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Genes Involved
Zebrafish Models