OBO ID: DOID:0080982
Term Name: X-linked mental retardation-hypotonic facies syndrome-1 Search Ontology:
Synonyms:
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 )
Relationships
is a type of:
OTHER X-linked mental retardation-hypotonic facies syndrome-1 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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