Human genes for chromosome 1p36 deletion syndrome
Chromosome 1p36 deletion syndrome [DOID:0060410]
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.
Synonyms: chromosome 1p36 deletion syndrome, chromosome 1p36 deletion disease, chromosome 1p36 deletion disorder, DOID:0060410, 1p36 deletion syndrome ...