OBO ID: DOID:0060397
Term Name: chromosome 15q26-qter deletion syndrome Search Ontology:
Synonyms:
  • 15q26 deletion syndrome
  • distal 15q deletion syndrome
  • distal monosomy 15q
  • Drayer syndrome
  • telomeric 15q deletion syndrome
Definition: A chromosomal deletion syndrome that is characterized by pre- and postnatal growth restriction, developmental delay, variable degrees of intellectual disability, brachy-clinodactyly, talipes equinovarus, nail hypoplasia, proximally placed digits and mild craniofacial dysmorphism including microcephaly, triangular face, broad nasal bridge and micrognathia. https://pubmed.ncbi.nlm.nih.gov/18651844
References:
Ontology: Human Disease   ( DOID:0060397 )
Relationships
is a type of:
OTHER chromosome 15q26-qter deletion syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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