Term Name:	chromosome 1p36 deletion syndrome
Synonyms:	1p36 deletion syndrome, deletion 1p36, monosomy 1p36, subtelomeric 1p36 deletion
Definition:	A chromosomal deletion syndrome that has_material_basis_in by deletion of the chromosome 1p36 region and is characterized by severe intellectual disability, a small head, deep-set eyes with straight eyebrows, midface hypoplasia, a broad, flat nose, a pointed chin and low-set ears.
Ontology:	Human Disease [DOID:0060410]   ( DOID:0060410 )