Human genes for chromosome 13q14 deletion syndrome
Chromosome 13q14 deletion syndrome [DOID:0060391]
A chromosomal deletion syndrome that is characterized by low birth weight, dysmorphic facies, limb defects, genital malformations and psychomotor developmental delay, has_material_basis_in deletion of the long arm of chromosome 13.
Synonyms: chromosome 13q14 deletion syndrome, chromosome 13q14 deletion disease, chromosome 13q14 deletion disorder, DOID:0060391, deletion 13q14