Search Ontology:
Human Disease
X-linked mental retardation-hypotonic facies syndrome-1
- Term ID
- DOID:0080982
- Synonyms
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- Definition
- A syndromic X-linked intellectual disability that is characterized primarily by severe mental retardation, dysmorphic facies, and a highly skewed X-inactivation pattern in carrier women and that has_material_basis_in mutation in the ATRX gene. X-linked mental retardation-hypotonic facies syndrome comprises several syndromes previously reported separately. These include Carpenter-Waziri, Holmes-Gang, and Smith-Fineman-Myers syndromes. X-linked alpha-thalassemia/mental retardation syndrome is an allelic disorder with a similar phenotype with the addition of alpha-thalassemia and Hb H inclusion bodies in erythrocytes. https://pubmed.ncbi.nlm.nih.gov/15508018/
- References
- Ontology
- Human Disease ( DOID:0080982 )
- is a type of
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Genes Involved
Zebrafish Models