Human genes for 3p deletion syndrome
3p deletion syndrome [DOID:0060417]
A chromosomal deletion syndrome that has_material_basis_in a contiguous gene deletion syndrome involving chromosome 3pter-p25 and is characterized by low birth weight, microcephaly, trigonocephaly, hypotonia, psychomotor and growth retardation, ptosis, telecanthus, downslanting palpebral fissures, and micrognathia.
Synonyms: 3p deletion syndrome, 3p deletion disease, 3p deletion disorder, DOID:0060417, chromosome 3pter-P25 deletion syndrome ...