DISEASES

Disease-gene associations mined from literature

Human genes for chromosome 9p deletion syndrome

Chromosome 9p deletion syndrome [DOID:0060732]

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.

Synonyms:  chromosome 9p deletion syndrome,  chromosome 9p deletion disease,  chromosome 9p deletion disorder,  DOID:0060732,  9p syndrome ...