Search Ontology:
Human Disease

chromosome 9p deletion syndrome

Term ID
DOID:0060732
Synonyms
  • 9p syndrome
  • Alfi syndrome
  • monosomy 9p syndrome
Definition
A chromosomal deletion syndrome characterized by trigonocephaly, flattened occiput midface hypoplasia, long philtrum, prominent forehead, broad flat nasal bridge, anteverted nares, malformed external ears, hypertelorism, hypertonia, delayed psychomotor development and that has_material_basis_in a contiguous gene deletion on the short arm of chromosome 9. (3)
References
Ontology
Human Disease   ( DOID:0060732 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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